A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3
© The Author(s). 2016
Received: 24 May 2016
Accepted: 17 July 2016
Published: 30 July 2016
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, or the congenital absence of uterus and vagina, is the most severe anomaly of the female reproductive tract. It affects 1 in 5,000 females, and is the second most common cause of primary amenorrhea. The etiology remains unknown in most patients, although four single gene defects and some repetitive copy number variants (CNVs) have been identified. Translocations in MRKH patients are very rare, and reported only in three patients previously without breakpoint mapping. We have identified the fourth MRKH translocation patient and are the first to characterize the breakpoints mapped by molecular methods.
The proband is a 17- year old white female with agenesis of the uterus and vagina who had a peripheral blood karyotype revealing a de novo balanced translocation 46,XX,t(3;16)(p22.3;p13.3)dn. There were no known related anomalies present in the proband or her family. No CNVs were found by chromosomal microarray analysis, and no genes were directly disrupted by the translocation. DNA sequencing of six nearby candidate genes—TRIM71, CNOT10, ZNF200, OR1F1, ZNF205, and ZNF213—did not reveal any mutations. RT-qPCR of proband lymphoblast RNA for 20 genes near the breakpoints of 3p22.3 and 16p13.3 showed significantly altered expression levels for four genes in the proband compared to three white female controls, after correction for multiple comparisons. Reduced expression was seen for CMTM7 and CCR4 on 3p22.3, while increased expression was observed for IL32 and MEFV on 16p13.3.
We have mapped the breakpoints of our t(3;16)(p22.3;p13.3) translocation patient using molecular methods to within 13.6 kb at 3p22.3 and within 1.9 kb for 16p13.3 and have suggested 10 nearby genes that become plausible candidate genes for future study.
Abnormal development of the uterus and vagina affects 7-10 % of women, comprising a significant cause of impaired reproductive function . Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also known as congenital absence of the uterus and vagina or mullerian aplasia, is the most severe anomaly of the female reproductive tract in which the uterus and vagina are absent from birth . MRKH (the name patients prefer) affects approximately 1 in 5,000 females, and is the second most common cause of primary amenorrhea . These women are 46,XX females that lack the vagina and most of the uterus, although fallopian tubes may be present . Ovaries are present with normal function, thus patients undergo spontaneous puberty.
MRKH is commonly classified with regard to the presence or absence of additional anomalies [2, 3]. Isolated agenesis of the uterus and vagina occurs in about two-thirds of MRKH patients, classified as Type I. The remaining one-third of MRKH patients have one or more associated anomalies, and are classified as Type II. More frequent associated anomalies involve the kidneys with renal agenesis (32 %) and the skeletal system (12 %) . Less commonly, women with MRKH may also present with deafness, inguinal hernia, or abnormalities of the cardiac or nervous systems .
While the etiology of MRKH is not well understood, disease clustering in >67 families clearly indicates a genetic component . A number of candidate genes including AMH, AMHR, WT1, WNT7A, CFTR, GALT, HOXA7, HOXA13, PBX1, HOXA10, RARG, RXRA, CTNNB1, PAX2, LAMC1, DLGH1, and SHOX have been screened for mutations in small numbers of MRKH patients, but no mutations were found [5–9]. Genomic regions 16p11 and 17q12 most commonly have been found to have copy number variants (CNVs) identified by chromosomal microarray analysis implicated in MRKH, but causation is difficult to prove [10, 11]. It is currently not clear if MRKH is a genomic disorder or if a single gene or several genes within these CNVs could be etiologic . Single gene defects have uncommonly been identified–only a few patients have WNT4 [12–15], LHX1 , HNF1B , or TBX6  gene mutations. The molecular basis for MRKH remains unknown in the vast majority of patients .
Patients with balanced translocations provide a unique and valuable opportunity to identify genes involved in human genetic disorders . The derivative chromosome breakpoint may disrupt or dysregulate genes, suggesting a genomic region of etiologic candidate genes . This method has been successful in identifying candidate genes in other disorders, and may be valuable to elucidating the molecular mechanisms of MRKH . Only three MRKH patients with balanced translocations have been reported in the literature, but fine mapping by molecular methods has not been performed for any of them [21, 22]. In this study we present an MRKH patient with a de novo balanced translocation of 46,XX,t(3;16)(p22.3;p13.3)dn with the purpose to: 1) identify the molecular breakpoints of 3p22 and 16p13; 2) propose candidate genes for MRKH; and 3) compare the proband to other MRKH patients with balanced translocations presented in the literature.
Six genes near the breakpoints were prioritized as reasonable candidate genes based upon either expression in appropriate tissues and/or proposed gene function. DNA sequencing was performed on genomic DNA from 51 MRKH patients for the protein coding exons and splice junctions for the two closest candidate genes near the breakpoint at 3p22.3---TRIM71 centromeric and CNOT10 telomeric. In addition, ZNF200, OR1F1, ZNF213, and ZNF205 at 16p13.3 were sequenced in 27 MRKH patients. No likely causative (nonsense, frameshift, or splice site) or potentially causative (nonsynonymous missense changes) variants were identified for any of these six genes.
Discussion and conclusions
The etiology of MRKH remains largely unknown [5, 24], although when families are examined, autosomal dominant or multifactorial/polygenic inheritance seems most likely . Several potentially causative repetitive CNVs have been described—most commonly deletions in 17q12 (n > 9) and 16p11 (n >5) , but it is not clear if they play a pathogenic role [5, 24]. Single gene defects are found even less commonly. To date, four WNT4 [12–15], one LHX1 , one HNF1B , and several TBX6  mutations and intragenic CNVs  have been characterized, indicating that many more genes for MRKH remain to be discovered.
While syndromic families have been reported, they are few and small in size . Thus their ability to show genetic segregation among affected family members is very limited. Most MRKH probands do not have a family history of other affected individuals. The inability of affected women to conceive and carry children is a significant barrier to characterizing inheritance patterns and identifying causative genes. However, when MRKH patients who underwent surrogacy were surveyed by a questionnaire, 32/53 (60 %) responded and 34 liveborns were delivered. Half were females, and only one child—a male—had a middle ear defect and hearing loss (1 of 17 = 5.9 %), consistent with an associated phenotype of MRKH . It is possible that less severe associated anomalies may not have been ascertained.
Genomic rearrangements, which include balanced translocations, occur more frequently than de novo point mutations, and may directly disrupt a gene, thereby altering its normal function, or result in a sufficient “position effect” to alter or impair its regulatory mechanisms.  Candidate genes suggested by this position effect have facilitated successful identification of causative mutations in multiple disorders, including PAX6 in aniridia, PITX2 in Reiger syndrome, FOXL2 in blepharophimosis/ptosis-epicanthus inversus syndrome, SOX9 in campomelic dysplasia, SRY in sex reversal, SIX3 in holoprosencephaly, and WDR11 in hypogonadotropic hypogonadism/Kallmann syndrome [20, 26]. Balanced translocations in affected individuals highlight a narrow section of the genome that is disrupted, and can provided much needed clues to the etiology of human disease .
Reported translocations in patients with MRKH
Kucheria et al. 
MRKH; renal agenesis
Amesse et al. 
46,XXt(8;13)(q22.1;q32.1) in blood; Mosaic in 4:1 ratio in buttock fibroblasts for minor cell line of 46,XX, t(1;12)(q23.1;q24.3),t(6;6)(q15;p25)
MRKH; congenital amastia/amelia,urinary reflux; urinary incontinence, megarethra
Williams et al.; Current case
Caucasian Northern European
In the current study, we mapped the molecular breakpoints in an MRKH female with a de novo 46,XX,t(3;16)(p22.3;p13.3)dn. A chromosomal microarray was used to narrow down the breakpoints of both derivative chromosomes to within 13.6 kb on der(3) and within 1.9 kb on der(16). No deletions/insertions were identified, which could have been potential confounders in this patient. No gene was directly disrupted, but the genes closest on either side of the breakpoint became prime positional candidate genes. We did not amplify and clone the breakpoints in this patient since the breakpoint region is not contained within a structural gene. TRIM71 (tripartite motif-containing 71) on the centromeric side of the breakpoint (Fig. 2) has been reported to be involved in the timing of organ formation during development , while CNOT10 on the telomeric side of the breakpoint is involved in transcription . We did not identify mutations in our available sample of 51 MRKH patients in these genes, which suggests they are not a common etiologic factor in MRKH. However, we cannot exclude that genes with mutation frequencies of 1-2 % could occur. We also performed DNA sequencing for three genes near the breakpoint on chromosome 16p13.3, namely OR1F1 on the centromeric side and three zinc finger genes involved in transcription—ZNF213 and ZNF205 on the telomeric side and ZNF200 on the centromeric side of the breakpoint. In 27 unrelated MRKH patients, no putative mutations were identified.
In addition, RNA was extracted from peripheral lymphoblastoid cells from our proband, and 20 genes near the breakpoints of both derivative chromosomes were subjected to RT-qPCR. Expression was normalized to the GAPDH reference gene and compared to three white female controls. Four genes were found to have statistically altered gene expression after correction for multiple comparisons. It is interesting that both genes on chromosome 3p22.3, CMTM7 and CCR4, have reduced expression, while both genes on 16p13.3, IL32 and MEFV, show increased expression. It is interesting to speculate whether the 3p genes regulate the 16p genes or vice versa. This will have to be determined experimentally in future studies. Two genes—CMTM7 and IL32—have the most profound differences, so they are the most plausible involved genes within the breakpoints.
Through the fine mapping of the breakpoints in this translocation patient, we have identified six candidate genes that require future testing based upon the location and proposed role in mullerian development—TRIM71 and CNOT10 on chromosome 3, and OR1F1, ZNF213, ZNF200, and ZNF205 on chromosome 16. By RT-qPCR, we show altered expression of four additional genes—CMTM7 and CCR4 on chromosome 3, and IL32 and MEFV on chromosome 16—that become reasonable candidate genes. Balanced chromosomal translocations may exert a position effect on genes within 10 kb or even up to a megabase away from the breakpoint . However, additional patients will need to be collected and studied to adequately test the hypothesis that these are involved in the pathogenesis of MRKH. Since deleterious gene mutations affecting most reproductive disorders usually occur at a frequency between 1-5 % [30, 31], large cohorts are necessary for sufficient power to identify new causative genes.
To date, balanced translocations from MRKH patients have not yielded causative genes in the etiology of the syndrome, but our more comprehensive molecular analysis of a t(3;16) translocation pinpoints specific chromosomal regions that will require further study. It is also certainly possible that causal variants could be localized outside the structural genes and might be detected by whole genome sequencing approaches. Nevertheless, the complicated genetic basis of MRKH remains unsolved, but study of large cohorts and families by innovative molecular approaches, appropriate in vitro confirmation of identified variants, and relevant mouse models will be necessary.
Our 52 patients with MRKH, except the proband with the t(3;16), were 46,XX females with adult (Tanner 5) breast development, normal pubic hair, and an absent vagina. Ultrasound or MRI was performed on some patients revealing hypoplasia or aplasia of the uterus. Associated anomalies were present in patients as follows: unilateral renal agenesis (n =7), skeletal anomalies (n = 6), cardiac defects (n = 3), and hearing loss (n = 5). All patients consented to have blood drawn for molecular analysis and signed a consent approved by the Human Assurance Committee of the Medical College of Georgia at Augusta University. LCL was funded by NIH HD33004 and the Department of Ob/Gyn at Augusta University, which were the sole sources of funding.
For breakpoint mapping, we did array painting essentially as described previously . Briefly, the EBV-transformed patient lymphoblastoid cell line was treated with colcemid, and metaphase chromosomes were then isolated and flow-sorted. Approximately 6,000 flow-sorted chromosomes were used directly for amplification with the GenomiPhi V2 DNA Amplification Kit (GE Healthcare, Piscataway, NJ, USA) according to the manufacturer’s recommendations. One microgram of amplified DNA from each derivative chromosome was labelled via Agilent´s Genomic DNA Enzymatic Labeling Kit Plus (Agilent). To each labelling reaction 100 ng of genomic control DNA were added to ensure proper placement of the grid for subsequent image analysis. These probes were hybridized to a custom array for high resolution breakpoint mapping. All hybridizations were done according to the manufacturer's recommendations for array CGH experiments (Agilent). Further analysis and visualization of array painting data was done using the array CGH software package CGHPRO .
Sanger DNA sequencing
DNA sequencing of all protein coding exons and splice junctions was performed on 51 MRKH patients for 4 exons in TRIM71 (NM_001039111.2) and 19 exons in CNOT10 (NM_015442.2) at the 3p22.3 breakpoint. In addition, 27 MRKH patient DNAs were subjected to Sanger sequencing for the 4 exons of ZNF200 (NM_003454.3), 1 exon of OR1F1 (NM_012360.1), 5 exons of ZNF213 (NM_004220.2), and 6 exons of ZNF205 (NM_001278158.1) at 16p13.3.
RNA was extracted from lymphoblastoid cells of the proband with the translocation and three white female controls using the TRI REAGENT (Molecular Research Center, Inc, Cincinnati, OH) standard protocol. RT-qPCR primers were designed with a product size of <155 bp for 20 genes around the chromosome 3 and chromosoms16 breakpoints. These genes included: CMTM6, CMTM7, CMTM8, DYNC1LI1, CNOT10, TRIM71, CCR4, GLB1, TMPPE, CRTAP, IL32, ZSCAN10, ZNF205, ZNF213, OR1F1, ZNF200, MEFV, ZNF263, TIGD7, and ZNF75A. GAPDH was used as the internal reference control.
The RT reaction was performed using the ABI-High Capacity cDNA Reverse Transcription Kit [RXN w/o RNAse Inhibitor] (Thermo Fisher Scientific, Waltham, MA). 2 μg of RNA were used in the 20 μl reaction with RT conditions of: 25 °C for 10 min, 37 °C for 120 min, 85 °C for 5 min, 4 °C cooling. The cDNA product was diluted 1:5 for the qPCR reaction, which was run on a Roche LightCycler 96 using the FastStart Essential DNA Green Master Kit protocol (Roche Diagnostics Corporation, Indianapolis, IN) with SYBR green. In the 25 μl reaction volume 2 μl of cDNA was used and each primer concentration was 25 pmol. GAPDH and each of the test genes were run in duplicate/run. Three separate experiments were performed. LightCycler 96 settings were: pre-incubation at 95 °C for 10 min, 3-step amplification (45 cycles of 95 °C 10 s, 60 °C 10 s, 72 °C 10 s), melting (95 °C 10 s, 65 °C 60 s, and 97 °C 1 s), and a final cooling at 37 °C for 30 s. CT values  and standard deviations were calculated and statistics were done using Z Score values with a Bonferroni correction. With the Bonferroni correction for 20 genes, a P <0.0025 was considered significant.
μg, microgram; μl, microliter; cDNA, complementary DNA; CGH, comparative genomic hybridization; CNVs, copy number variants; der(16), derivative chromosome 16; der(3), derivative chromosome 3; DNA, deoxyribonucleic acid; EBV, Epstein Barr virus; kb, kilobase; min, minute; MRKH, Mayer-Rokitansky-Kuster-Hauser syndrome; pmol, picomole; qPCR, quantitative polymerase chain reaction; RNA, ribonucleic acid; RT-qPCR, real time-quantitative polymerase chain reaction; t(3;16), translocation of chromosomes 3 and 16
LCL was funded by NIH HD33004 and the Department of Ob/Gyn at Augusta University.
Availability of data and materials
We do not believe there is any relevant data of interest to share as there are no unique cell lines, software, or databases.
LW wrote the paper and performed DNA sequencing of candidate genes. HK and VK collaborated to perform the positional cloning to identify the breakpoint regions. JT, LC, ME, and AF performed DNA sequencing on the different candidate genes. LC and ME also performed RT-qPCR on the 20 candidate genes from lymphoblast RNA. RR identified and characterized the MRKH patient and obtained the pedigree and samples on the family members and edited the final manuscript. LL oversaw all aspects of the manuscript, funded the project, edited the final manuscript, and is the corresponding author. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
All patients consented to have blood drawn for molecular analysis and signed a consent approved by the Human Assurance Committee of the Medical College of Georgia at Augusta University.
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- Reindollar RH, Byrd JR, McDonough PG. Delayed sexual development:study of 252 patients. Am J Obstet Gynecol. 1981;140:371–80.View ArticlePubMedGoogle Scholar
- Morcel K, Guerrier D, Watrin T, Pellerin I, Leveque J. The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: clinical description and genetics. J Gynecol Obstet Biol Reprod (Paris). 2008;37:539–46.View ArticleGoogle Scholar
- Oppelt P, Renner SP, Kellermann A, et al. Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging. Hum Reprod. 2006;21:792–7.View ArticlePubMedGoogle Scholar
- Herlin M, Hojland AT, Petersen MB. Familial occurrence of Mayer-Rokitansky-Kuster-Hauser syndrome: a case report and review of the literature. Am J Med Genet A. 2014;164A:2276–86.View ArticlePubMedGoogle Scholar
- Layman LC. The genetics of mullerian aplasia. Expert Rev Endocrinol Metab. 2014;9:411–9.View ArticleGoogle Scholar
- van Lingen BL, Reindollar RH, Davis AJ, Gray MR. Further evidence that the WT1 gene does not have a role in the development of the derivatives of the mullerian duct. Am J Obstet Gynecol. 1998;179:597–603.View ArticlePubMedGoogle Scholar
- Resendes BL, Sohn SH, Stelling JR, et al. Role for anti-Mullerian hormone in congenital absence of the uterus and vagina. Am J Med Genet. 2001;98:129–36.View ArticlePubMedGoogle Scholar
- Timmreck LS, Gray MR, Handelin B, et al. Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina. Am J Med Genet A. 2003;120A:72–6.View ArticlePubMedGoogle Scholar
- Timmreck LS, Pan HA, Reindollar RH, Gray MR. WNT7A mutations in patients with Mullerian duct abnormalities. J Pediatr Adolesc Gynecol. 2003;16:217–21.View ArticlePubMedGoogle Scholar
- Cheroki C, Krepischi-Santos AC, Szuhai K, et al. Genomic imbalances associated with mullerian aplasia. J Med Genet. 2008;45:228–32.View ArticlePubMedGoogle Scholar
- Nik-Zainal S, Strick R, Storer M, et al. High incidence of recurrent copy number variants in patients with isolated and syndromic Mullerian aplasia. J Med Genet. 2011;48:197–204.View ArticlePubMedPubMed CentralGoogle Scholar
- Biason-Lauber A, De Filippo G, Konrad D, Scarano G, Nazzaro A, Schoenle EJ. WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Hum Reprod. 2007;22:224–9.View ArticlePubMedGoogle Scholar
- Biason-Lauber A, Konrad D, Navratil F, Schoenle EJ. A WNT4 mutation associated with Mullerian-duct regression and virilization in a 46, XX woman. N Engl J Med. 2004;351:792–8.View ArticlePubMedGoogle Scholar
- Philibert P, Biason-Lauber A, Gueorguieva I, et al. Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Kuster-Hauser syndrome). Fertil Steril. 2011;95:2683–6.View ArticlePubMedGoogle Scholar
- Philibert P, Biason-Lauber A, Rouzier R, et al. Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and mullerian duct abnormalities: a French collaborative study. J Clin Endocrinol Metab. 2008;93:895–900.View ArticlePubMedGoogle Scholar
- Ledig S, Brucker S, Barresi G, Schomburg J, Rall K, Wieacker P. Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. Hum Reprod. 2012;27:2872–5.View ArticlePubMedGoogle Scholar
- Lindner TH, Njolstad PR, Horikawa Y, Bostad L, Bell GI, Sovik O. A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta. Hum Mol Genet. 1999;8:2001–8.View ArticlePubMedGoogle Scholar
- Sandbacka M, Laivuori H, Freitas E, et al. TBX6, LHX1 and copy number variations in the complex genetics of Mullerian aplasia. Orphanet J Rare Dis. 2013;8:125.View ArticlePubMedPubMed CentralGoogle Scholar
- Dobek WA, Kim HG, Walls CA, et al. Long-term follow-up of females with unbalanced X Y translocations-reproductive and nonreproductive consequences. Mol Cytogenet. 2015;8:13.View ArticlePubMedPubMed CentralGoogle Scholar
- Kleinjan DA, van Heyningen V. Long-range control of gene expression: emerging mechanisms and disruption in disease. Am J Hum Genet. 2005;76:8–32.View ArticlePubMedGoogle Scholar
- Kucheria K, Taneja N, Kinra G. Autosomal translocation of chromosomes 12q & 14q in mullerian duct failure. Indian J Med Res. 1988;87:290–2.PubMedGoogle Scholar
- Amesse L, Yen FF, Weisskopf B, Hertweck SP. Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation. Clin Genet. 1999;55:493–5.View ArticlePubMedGoogle Scholar
- Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008;3:1101–8.View ArticlePubMedGoogle Scholar
- Sultan C, Biason-Lauber A, Philibert P. Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings. Gynecol Endocrinol. 2009;25:8–11.View ArticlePubMedGoogle Scholar
- Petrozza JC, Gray MR, Davis AJ, Reindollar RH. Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: outcomes of surrogate pregnancies. Fertil Steril. 1997;67:387–9.View ArticlePubMedGoogle Scholar
- Kim HG, Ahn JW, Kurth I, et al. WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Am J Hum Genet. 2010;87:465–79.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim HG, Herrick SR, Lemyre E, et al. Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1. J Med Genet. 2005;42:666–72.View ArticlePubMedPubMed CentralGoogle Scholar
- Maller Schulman BR, Liang X, Stahlhut C, DelConte C, Stefani G, Slack FJ. The let-7 microRNA target gene, Mlin41/Trim71 is required for mouse embryonic survival and neural tube closure. Cell Cycle. 2008;7:3935–42.View ArticlePubMedGoogle Scholar
- Mauxion F, Preve B, Seraphin B. C2ORF29/CNOT11 and CNOT10 form a new module of the CCR4-NOT complex. RNA Biol. 2013;10:267–76.View ArticlePubMedPubMed CentralGoogle Scholar
- Layman LC. The genetic basis of female reproductive disorders: Etiology and clinical testing. Mol Cell Endocrinol. 2013;370:138–48.View ArticlePubMedPubMed CentralGoogle Scholar
- Layman LC. Clinical genetic testing for kallmann syndrome. J Clin Endocrinol Metab. 2013;98:1860–2.View ArticlePubMedPubMed CentralGoogle Scholar
- Kalscheuer VM, FitzPatrick D, Tommerup N, et al. Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation. Hum Genet. 2007;121:501–9.View ArticlePubMedGoogle Scholar
- Chen W, Erdogan F, Ropers HH, Lenzner S, Ullmann R. CGHPRO -- a comprehensive data analysis tool for array CGH. BMC Bioinformatics. 2005;6:85.View ArticlePubMedPubMed CentralGoogle Scholar