Rate of vertical transmission of human papillomavirus from mothers to infants: Relationship between infection rate and mode of delivery
- Hyun Park†1,
- Si Won Lee†2,
- In Ho Lee2,
- Hyun Mee Ryu2,
- A Reum Cho3,
- Young Soon Kang4,
- Sung Ran Hong5,
- Sung Soon Kim6,
- Seok Ju Seong7,
- Son Moon Shin8 and
- Tae Jin Kim2Email author
© Park et al.; licensee BioMed Central Ltd. 2012
Received: 13 October 2011
Accepted: 12 April 2012
Published: 12 April 2012
In contrast to consistent epidemiologic evidence of the role of sexual transmission of human papillomavirus (HPV) in adults, various routes may be related to HPV infection in infants. We have assessed the extent of HPV infection during the perinatal period, and the relationship between mode of delivery and vertical transmission.
A total of 291 pregnant women over 36 weeks of gestation were enrolled with informed consent. Exfoliative cells were collected from maternal cervix and neonatal buccal mucosa. HPV infection and genotypes were determined with an HPV DNA chip, which can recognise 24 types. The HPV-positive neonates were re-evaluated 6 months after birth to identify the presence of persistent infection. HPV DNA was detected in 18.9 % (55/291) of pregnant women and 3.4 % (10/291) of neonates. Maternal infection was associated with abnormal cytology (p = 0.007) and primiparity (p = 0.015). The infected neonates were all born to HPV-positive mothers. The rate of vertical transmission was estimated at 18.2 % (10/55) which was positively correlated with maternal multiple HPV infection (p = 0.003) and vaginal delivery (p = 0.050), but not with labour duration and premature rupture of membranes. The rate of concordance of genotype was 100 % in mother-neonate pairs with vertical transmission. The neonatal HPV DNAs found at birth were all cleared at 6 months after delivery.
Vertical transmission of HPV DNA from HPV infected mother to the neonate increased when the infant was delivered through an infected cervix. However, the absence of persistent infection in infants at 6 months after delivery may suggest temporary inoculation rather than true vertical infection.
Approximately 200 different genotypes of human papillomavirus (HPV) have been identified and >40 types are associated with anogenital diseases . While these mucosal types are suspected of affecting predominantly adults, reports of HPV related diseases in the oropharyngeal and anogenital mucosa of infants and children born to HPV infected mothers are increasing .
In contrast to the consistent epidemiologic reports, including the role of sexual transmission of HPV in adults , potential routes of HPV infection from mother to newborns were as follows: 1) during passage of the fetus through an infected birth canal, 2) ascending infection after premature rupture of the membranes, 3) infected sperm at fertilization, and 4) hematogenous spread .
The extent and risk factors of HPV infections in infants have been controversial. For pregnant women and their babies, the only meta-analysis to date show that vertical transmission developed in one-third of neonates born to infected mothers mainly through vaginal deliveries . However, there was a wide variation in the rate of vertical transmission ranging from 0-80 % [4, 6–9]. Furthermore, a report with type-specific polymerase chain reaction (PCR) or DNA sequencing has identified the lack of concordance of HPV genotypes in 57-69 % of the mother-neonate pairs . The discrepancy is regarded as evidence proposing various routes of viral transmission other than the birth canal.
HPV DNA chip and PCR-based oligonucleotides microarray have been useful in many screening programs for the early diagnosis of cervical dysplasia and cancer . This technique can accurately determine HPV-positivity and distinguish types of HPV DNA, even in cases infected with multiple types . In addition to potential factors associated with neonatal infection, HPV genotying can be helpful in explaining the mechanism of viral transmission.
In this study, we have determined the prevalence of HPV infection in pregnant women and the rate of vertical transmission during the perinatal period. The risk factors associated with viral transmission were also explored, including HPV genotypes.
A total of 300 term pregnant women were enrolled over the study period. Analyses were restricted to 291 women who gave birth in the institutes through vaginal delivery (n = 193, 66.3 %) and caesarean section (n = 98, 33.7 %).
Maternal HPV status
The mean age of pregnant women was 32.8 years and the prevalence of HPV infection was 18.9 % (55/291) in maternal cervical swabs at enrolment determined by means of HPV DNA chips. In the cytology performed at the first trimester, 283 women were negative for intraepithelial lesions and 8 had atypical squamous cells of undetermined significance. Women with abnormal cytology were referred for colposcopic examination and the results indicated no dysplasia in the cervix. Prevalence of HPV infection in the newborns was 3.4 % (10/291) from swabs of oral mucosa at delivery.
Characteristics associated with maternal HPV status
Bacterial genital infection
Among the types specified by HPV DNA chip, HPV-16 was the most frequent type in the maternal cervix (n = 55), comprising 8 cases (14.5 %) and other specified HPV types were as follows: HPV-6, -56 each in 5 cases (9.1 %); -53, -58, -70 each in 4 cases (7.3 %); -39, -40 each in 3 cases (5.5 %); and −44, -51, -31 each in 2 cases (3.6 %). Each of HPV-11, -18, -33, -35, -45, and −66 was noted only in one participant. HPV-other type, which was positive in PCR but negative in HPV DNA chip, was noted in 29.1 % (16/55). Genotyping showed that 58.2 % (32/55) were infected with at least one type of high-risk HPVs.
Co-infection with multiple genotypes was noted in 8 mothers; 3 mothers were infected with 3 types, and 5 with 2. HPV-53 (n = 4) was the most frequent type found in multiple infection. HPV-40 was detected in 3 cases and HPV-44 and −56 were detected in 2 cases. HPV-11, -16, -33, -35, -58, -66 and −68 were detected once.
Neonatal HPV status
Concordance of HPV genotypes in mother-neonate pairs
at day 0
at 6 months
40, 44, 53
40, 44, 53
58, 31, 68
Factors associated with vertical transmission
The reproductive characteristics associated with neonatal HPV status
(SD or %)
(SD or %)
Gestational age (w)
Length of labour(min) (n = 45)
Mode of delivery
Risk of HPV type
LR or other type
Number of HPV type
Discussion and conclusions
The prevalence and concordance of HPV infection in mother neonate pairs by HPV genotype detection has been investigated. Comparison of HPV genotypes in relation to obstetric characteristics lead us to suggest the primary route of vertical transmission during perinatal period. According to epidemiological data of HPV infection in the female population, HPV prevalence ranges from 10 % in women with normal cytology to nearly 100 % in women with cervical cancer [3, 12, 13]. In addition to cervical disease, the age, region, HPV detection method and study design are also associated with the estimates of HPV infection .
For pregnant women, the percentage positivity varied from 5.5 to 65 % using the only meta-analysis to date . Outstandingly high estimates tend to be reported by research conducted in an endemic area or for high risk participants identified with the pathos-mechanism of vertical transmission. Up to 60 % of young pregnant women were infected with HPV in Uganda, where a similar frequency was reported in non-pregnant women . In contrast, a lower prevalence has been reported by large cohort studies of the general population. A recent study in Spain surveyed 828 women who were consecutively included at the perinatal clinic and found 6.5 % to be infected with HPV . A study by Takakuwa et al. , one of the largest (n = 1183), presented an overall prevalence of 12.5 %, with the prevalence in women under 25 years of age being significantly higher compared than in women over 25 years (22.6 vs. 11.3 %, p < 0.0005).
The present study has shown the prevalence of HPV infection of the cervix to be 18.9 % in 291 Korean pregnant women without abnormal cervical lesion under colposcopy, which was comparable to those of large studies mentioned above. The infection was more frequently detected in women with abnormal cytology and without a history of parturition. Although statistically insignificant, young women under 30 years of age were more infected with HPV (Table 1).
Age is constantly reported to be related to the proportion of positive findings in pregnant women, as in non-pregnant women. Eppel et al.  showed decreased prevalence of HPV infection with increasing maternal age. The group younger than 30 years had twice the risk risk of the group older than 30 years. In young women, HPV infection is transient, which is considered to be one of the mechanisms explaining why the finding of HPV after the age of 25 or 30 years is less frequent .
Since Sedlacek et al.  detected HPV DNA in neonatal oropharyngeal aspirates , widely variable estimates of perinatal HPV infection have been reported in terms of neonatal prevalence, frequency of vertical transmission, and persistent infection. Their inconsistent results depend on selection criteria, sample size, period of follow-up and particularly the method of assay.
A higher rate of vertical transmission, 70-80 %, came from early small studies when analyzing methods for HPV DNA detection by PCR were still developing [9, 20]. While PCR is known to be the most sensitive method and type-specific PCR can detect <10 copies of HPV DNA, this technique can give false-positives due to contamination, as it relies on a series of laboratory preparations for target amplification . DNA sequencing, another highly sensitive method, can verify the genotype and reduce the probability of false-positives by sequencing. Smith et al.  were the first to sequence a number of HPV genotypes and reported that only 3.7 % (6/164) of neonates were positive for HPV DNA. However, this technique alone is unable to identify each viral type in multiple infections.
In our study, vertical transmission was found in 18.5 % (10/55) with HPV DNA chip, which can identify genotypes even in the cases with multiple infections through automated and efficient procedures. This technique is appropriate for large epidemiological studies and its efficacy for genotyping of HPV infection has been demonstrated in cervical cancer screening programs [10, 11]. Our results are supported by the fact that research since 2000 has reported similar estimates ranging from 10-20 %, using strong laboratory methods that can genotype a number of HPVs [15, 22, 23].
We could add some data to the current consensus that HPV in a neonate was probably acquired during the passage through an infected cervix . The genotypes were concordant in the mother newborn pairs with vertical transmission that made us infer the source of HPV infection (Table 2). In addition, 10 newborns with positive HPV were delivered vaginally (Table 3). Tenti et al.  reported very similar data that HPV DNA was positive only in babies delivered through the infected birth canal, and that the genotypes of the pairs were identical to each other.
However, many studies also presented biological evidence suggesting other possible routes of viral transmission. HPV DNAs have been detected in sperm, amniotic fluid, placenta, cord and maternal blood [24–26]. Further, the concordance of HPV types between mothers and newborns is 57-69 % and HPV-positive newborns having HPV-negative mothers have been reported . These results propose that some newborns can acquire HPV DNA through horizontal transmission from other contact after birth or in uterine transmission at an untested interval during early pregnancy.
In pregnant women, a few studies have assessed the extent of multiple infections, which is considered uncommon. With the introduction of laboratory techniques that can simultaneously identify multiple types of HPV, some investigators have reported that co-infection was detected in 17-66 % of the infected women [15, 22, 23]. Several studies have attempted to picture the association of multiple infections with vertical transmission. Tseng et al.  could distinguish only 2 types (HPV-16, -18) with PCR and reported that vertical transmission developed in 4 out of 11 women with double infection and 23 out of 57 with single infections. Rombaldi et al.  used the novel nested multiplex PCR with an ability to differentiate 19 types and showed that each 4 cases of vertical transmission occurred in 19 pairs with single infection and 30 with multiple infections. In this report, we demonstrated that multiple infection had a significantly higher probability of transmitting to newborns than a single infection (5/8 vs. 5/47, p = 0.003) (Table 3).
It has been argued whether or not the detection of HPV DNA after birth reflects a true infection or contamination. Because HPV infection has a long latent period, the repeated detection of HPV in the same area is considered as persistent infection. Some early studies used PCR and serially detected HPV DNA in the buccal and genital swabs at birth and at weeks to months of postpartum. Cason et al.  demonstrated that HPV-16 DNA persisted for up to 6 months in 80 % of HPV positive infants at birth. Kaye et al.  showed HPV-16 in the samples by sequencing analysis from 13 maternal cervices, and from their infants at 6 weeks and 2 years of age. The concordance was estimated to be 69.2 % and at least 15.4 % of infants maintained maternally-derived HPV infections until 2 years. In contrast to previous studies, we were unable to detect any persistent infection at 6 months in HPV positive newborns (Table 2). A prospective study reported that the virus was cleared in all infants as early as the 5th week during follow-up period until 18 months . In a cohort study of Finnish families, the risk of infant HPV was not cervical HPV during pregnancy, but persistent maternal HPV infection . These results indicate that vertical transmission at birth may not contribute to persistent infection in infants.
As commented in previous literature reviews, the estimates should be interpreted with caution in respect of geographic and demographic characteristics, research design, and detection methods of HPV [2, 5, 12]. Because our participants were consecutively included at one of the largest obstetric clinics in Korea where over 5000 newborns are delivered in a year, our estimates are presumed to have credable generality. In order to ascertain the persistency of HPV infection, we followed up the infants until 6 month postpartum, which was scarcely covered by previous studies [5, 30]. We also discriminated over 24 HPV genotypes to evaluate the concordance with DNA chip, which is the one of the largest spectrums to date. Whilst HPV DNA chip is as efficient as the existing HPV detection methods, a recent study pointed out its limit of usefulness as a screening tool due to low sensitivity . The combined use of advanced diagnostic procedures will allow a more accurate assessment of extent of HPV infection in pregnant women and newborns in further studies .
In conclusion, the infection and transmission of HPV was prevalent in pregnant women and their neonates. We suggest that the perinatal transmission of HPV takes place through an infected birth canal based on the concordance of HPV genotypes and the predominance of vaginal delivery. However, the clearance of HPV in all infants up to 6 months suggests that HPV DNAs of newborns do not indicate persistent infection in infants.
This prospective study was approved by the institution’s ethics committee. Near term pregnant women anticipating deliveries at the department of obstetrics in a university affiliated hospital were recruited between April 2010 and January 2011. Participants fully understood the protocol of this study and signed written consent forms.
Pregnant women over 36 weeks gestation were included. Exclusion criteria were as follows: severe intra-uterine growth restriction, severe oligohydroamnios or preterm premature rupture of membranes, severe hypertension during pregnancy, history of malignancies within 5 years, liver cirrhosis, renal failure, chronic diseases affecting maternofetal immunity and a history of psychological disease and alcoholism. On the day of admission for delivery, newborns of the participants were enrolled after maternal re-consent.
At enrolment, cervical swabs were taken of the pregnant participants. Exfoliative cervical cells were collected using cytobrush for HPV DNA chip analysis. Immediately after delivery, the oral mucosa of newborns was scraped for HPV DNA chip analysis. The test was repeated at 6 month postpartum for HPV-positive infants to identify persistent infection.
HPV DNA genotyping
HPV detection and genotyping was performed using the HPV DNA Chip, PCR-based DNA microarray system, purchased from MyGene Company (Seoul, South Korea). The HPV DNA Chip contains 24 type specific probes; 15 types from the high-risk group (HPV-16, HPV-18, HPV-31, HPV-33, HPV-35, HPV-39, HPV-45, HPV-51, HPV-52, HPV-53, HPV-56, HPV-58, HPV-59, HPV-66, and HPV-68) and 9 types from the low-risk groups (HPV-6, HPV-11, HPV-34, HPV-40, HPV-42, HPV-43, HPV-44, HPV-54, and HPV-70). Briefly, DNA was isolated from swab samples using a DNA isolation kit (MyGene. Co, Seoul, Korea), and target L1 regions of HPV DNA were amplified using consensus GPd5+/GP6day + primers. Ten μlof the HPV-amplified product was denatured for 5 min at 95°C. The samples were mixed with a hybridization solution then applied onto the DNA Chip.
Hybridized HPV DNA was visualized using a DNA Chip scanner (Scanarray lite; GSI Lumonics®, Ottawa, Ontario, Canada). HPV amplicons can be hybridized with the corresponding type-specific oligonucleotide probe and visualized on HPV DNA Chip slides as double-positive spots when HPV DNA is present in amplified PCR product.
The samples that showed a positive band of 150 bp on the gel electrophoresis, but were negative on the HPV DNA Chip slide, were designated as HPV-other. None of the negative controls (without DNA) revealed HPV positivity.
To identify the factors associated with HPV infection in pregnant women and neonates, participants were assigned into 2 groups according to the presence or absence of HPV. Continuous variables were compared with Student’s t-test and discrete with chi-square test or Fisher’s exact test. The Mantel-Haenszel test was used to control for the confounding from age to some factors which were significantly associated with maternal HPV status under univariate analyses. P < 0.05 was considered significant with the use of a 2-sided test.
This study was supported by a grant of Korea Centres for Disease Control and Prevention (No. 2010-E51007-00).
- Garland SM: Human papillomavirus update with a particular focus on cervical disease. Pathology 2002, 34: 213-224. 10.1080/00313020212469PubMedView ArticleGoogle Scholar
- Syrjanen S, Puranen M: Human papillomavirus infections in children: the potential role of maternal transmission. Crit Rev Oral Biol Med 2000, 11: 259-274. 10.1177/10454411000110020801PubMedView ArticleGoogle Scholar
- Schiffman M, Castle PE, Jeronimo J, Rodriguez AC, Wacholder S: Human papillomavirus and cervical cancer. Lancet 2007, 370: 890-907. 10.1016/S0140-6736(07)61416-0PubMedView ArticleGoogle Scholar
- Tseng CJ, Liang CC, Soong YK, Pao CC: Perinatal transmission of human papillomavirus in infants: relationship between infection rate and mode of delivery. Obstet Gynecol 1998, 91: 92-96. 10.1016/S0029-7844(97)00593-0PubMedView ArticleGoogle Scholar
- Medeiros LR, Ethur AB, Hilgert JB, Zanini RR, Berwanger O, Bozzetti MC, Mylius LC: Vertical transmission of the human papillomavirus: a systematic quantitative review. Cad Saude Publica 2005, 21: 1006-1015.PubMedView ArticleGoogle Scholar
- Smith EM, Ritchie JM, Yankowitz J, Swarnavel S, Wang D, Haugen TH, Turek LP: Human papillomavirus prevalence and types in newborns and parents: concordance and modes of transmission. Sex Transm Dis 2004, 31: 57-62. 10.1097/01.OLQ.0000105327.40288.DBPubMedView ArticleGoogle Scholar
- Watts DH, Koutsky LA, Holmes KK, Goldman D, Kuypers J, Kiviat NB, Galloway DA: Low risk of perinatal transmission of human papillomavirus: results from a prospective cohort study. Am J Obstet Gynecol 1998, 178: 365-373. 10.1016/S0002-9378(98)80027-6PubMedView ArticleGoogle Scholar
- Tenti P, Zappatore R, Migliora P, Spinillo A, Belloni C, Carnevali L: Perinatal transmission of human papillomavirus from gravidas with latent infections. Obstet Gynecol 1999, 93: 475-479. 10.1016/S0029-7844(98)00459-1PubMedView ArticleGoogle Scholar
- Cason J, Kaye JN, Jewers RJ, Kambo PK, Bible JM, Kell B, Shergill B, Pakarian F, Raju KS, Best JM: Perinatal infection and persistence of human papillomavirus types 16 and 18 in infants. J Med Virol 1995, 47: 209-218. 10.1002/jmv.1890470305PubMedView ArticleGoogle Scholar
- Hwang TS, Jeong JK, Park M, Han HS, Choi HK, Park TS: Detection and typing of HPV genotypes in various cervical lesions by HPV oligonucleotide microarray. Gynecol Oncol 2003, 90: 51-56. 10.1016/S0090-8258(03)00201-4PubMedView ArticleGoogle Scholar
- Choi YD, Jung WW, Nam JH, Choi HS, Park CS: Detection of HPV genotypes in cervical lesions by the HPV DNA Chip and sequencing. Gynecol Oncol 2005, 98: 369-375. 10.1016/j.ygyno.2005.04.044PubMedView ArticleGoogle Scholar
- de Sanjose S, Diaz M, Castellsague X, Clifford G, Bruni L, Munoz N, Bosch FX: Worldwide prevalence and genotype distribution of cervical human papillomavirus DNA in women with normal cytology: a meta-analysis. Lancet Infect Dis 2007, 7: 453-459. 10.1016/S1473-3099(07)70158-5PubMedView ArticleGoogle Scholar
- Kim YT: Current status of cervical cancer and HPV infection in Korea. J Gynecol Oncol 2009, 20: 1-7. 10.3802/jgo.2009.20.1.1PubMedPubMed CentralView ArticleGoogle Scholar
- Banura C, Franceschi S, van Doorn LJ, Arslan A, Kleter B, Wabwire-Mangen F, Mbidde EK, Quint W, Weiderpass E: Prevalence, incidence and clearance of human papillomavirus infection among young primiparous pregnant women in Kampala, Uganda. Int J Cancer 2008, 123: 2180-2187. 10.1002/ijc.23762PubMedView ArticleGoogle Scholar
- Castellsague X, Drudis T, Canadas MP, Gonce A, Ros R, Perez JM, Quintana MJ, Munoz J, Albero G, de Sanjose S, Bosch FX: Human Papillomavirus (HPV) infection in pregnant women and mother-to-child transmission of genital HPV genotypes: a prospective study in Spain. BMC Infect Dis 2009, 9: 74. 10.1186/1471-2334-9-74PubMedPubMed CentralView ArticleGoogle Scholar
- Takakuwa K, Mitsui T, Iwashita M, Kobayashi I, Suzuki A, Oda T, Torii Y, Matsumoto M, Yahata G, Tanaka K: Studies on the prevalence of human papillomavirus in pregnant women in Japan. J Perinat Med 2006, 34: 77-79.PubMedGoogle Scholar
- Eppel W, Worda C, Frigo P, Ulm M, Kucera E, Czerwenka K: Human papillomavirus in the cervix and placenta. Obstet Gynecol 2000, 96: 337-341. 10.1016/S0029-7844(00)00953-4PubMedView ArticleGoogle Scholar
- Ho GY, Bierman R, Beardsley L, Chang CJ, Burk RD: Natural history of cervicovaginal papillomavirus infection in young women. N Engl J Med 1998, 338: 423-428. 10.1056/NEJM199802123380703PubMedView ArticleGoogle Scholar
- Sedlacek TV, Lindheim S, Eder C, Hasty L, Woodland M, Ludomirsky A, Rando RF: Mechanism for human papillomavirus transmission at birth. Am J Obstet Gynecol 1989, 161: 55-59.PubMedView ArticleGoogle Scholar
- Puranen MH, Yliskoski MH, Saarikoski SV, Syrjanen KJ, Syrjanen SM: Exposure of an infant to cervical human papillomavirus infection of the mother is common. Am J Obstet Gynecol 1997, 176: 1039-1045. 10.1016/S0002-9378(97)70399-5PubMedView ArticleGoogle Scholar
- Iftner T, Villa LL: Chapter 12: Human papillomavirus technologies. J Natl Cancer Inst Monogr 2003, 31: 80-88.PubMedView ArticleGoogle Scholar
- Bandyopadhyay S, Sen S, Majumdar L, Chatterjee R: Human papillomavirus infection among Indian mothers and their infants. Asian Pac J Cancer Prev 2003, 4: 179-184.PubMedGoogle Scholar
- Rombaldi RL, Serafini EP, Mandelli J, Zimmermann E, Losquiavo KP: Transplacental transmission of Human Papillomavirus. Virol J 2008, 5: 106. 10.1186/1743-422X-5-106PubMedPubMed CentralView ArticleGoogle Scholar
- Lai YM, Yang FP, Pao CC: Human papillomavirus deoxyribonucleic acid and ribonucleic acid in seminal plasma and sperm cells. Fertil Steril 1996, 65: 1026-1030.PubMedGoogle Scholar
- Armbruster-Moraes E, Ioshimoto LM, Leao E, Zugaib M: Presence of human papillomavirus DNA in amniotic fluids of pregnant women with cervical lesions. Gynecol Oncol 1994, 54: 152-158. 10.1006/gyno.1994.1185PubMedView ArticleGoogle Scholar
- Sarkola ME, Grenman SE, Rintala MA, Syrjanen KJ, Syrjanen SM: Human papillomavirus in the placenta and umbilical cord blood. Acta Obstet Gynecol Scand 2008, 87: 1181-1188. 10.1080/00016340802468308PubMedView ArticleGoogle Scholar
- Tseng CJ, Lin CY, Wang RL, Chen LJ, Chang YL, Hsieh TT, Pao CC: Possible transplacental transmission of human papillomaviruses. Am J Obstet Gynecol 1992, 166: 35-40.PubMedView ArticleGoogle Scholar
- Kaye JN, Starkey WG, Kell B, Biswas C, Raju KS, Best JM, Cason J: Human papillomavirus type 16 in infants: use of DNA sequence analyses to determine the source of infection. J Gen Virol 1996,77(Pt 6):1139-1143.PubMedView ArticleGoogle Scholar
- Rintala MA, Grenman SE, Puranen MH, Isolauri E, Ekblad U, Kero PO, Syrjanen SM: Transmission of high-risk human papillomavirus (HPV) between parents and infant: a prospective study of HPV in families in Finland. J Clin Microbiol 2005, 43: 376-381. 10.1128/JCM.43.1.376-381.2005PubMedPubMed CentralView ArticleGoogle Scholar
- Koskimaa HM, Waterboer T, Pawlita M, Grenman S: Syrjanen K. Human Papillomavirus Genotypes Present in the Oral Mucosa of Newborns and their Concordance with Maternal Cervical Human Papillomavirus Genotypes. J Pediatr, Syrjanen S; 2011.Google Scholar
- Um TH, Lee EH, Chi HS, Kim JW, Hong YJ, Cha YJ: Comparison of HPV genotyping assays and Hybrid Capture 2 for detection of high-risk HPV in cervical specimens. Ann Clin Lab Sci 2011, 41: 48-55.PubMedGoogle Scholar
- Tinelli A, Leo G, Dell'Edera D, Storelli F, Galante MM, Guido M, Hudelist G, Malvasi A: Molecular methods for a correct diagnosis of multiple HPV infections and clinical implications for vaccine. Int J Gynecol Cancer 2011, 21: 545-550. 10.1097/IGC.0b013e31820f5eedPubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.