Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).
about
Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeMayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findingsCandidate gene analysis in a case of congenital absence of the endometrium.Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association).A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patientsGene expression profile of patients with Mayer-Rokitansky-Küster-Hauser syndrome: new insights into the potential role of developmental pathways.Mayer-rokitansky-kuster-hauser syndrome: surgical management of two cases.Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.Molecular analysis of the beta-catenin gene in patients with the Mayer-Rokitansky-Küster-Hauser syndrome.Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.Müllerian duct anomalies: review of current management.Sequence variants in ESR1 and OXTR are associated with Mayer-Rokitansky-Küster-Hauser syndrome.Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.Mullerian dysgenesis: a critical review of the literature.Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.Congenital Malformations of the Reproductive Tract in a Patient with Poland Syndrome: Is There a Connection?Intensive vaginal dilation using adjuvant treatments in women with Mayer-Rokitansky-Kuster-Hauser syndrome: retrospective cohort study.SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.Gonadal agenesis with hypoplastic paramesonephric ducts (PMNDs) derivatives in dizygotic twins.Etiologies of uterine malformations.Discordant Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome in identical twins - a case report and implications for reproduction in MRKH women.
P2860
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P2860
Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).
description
2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina)
@nl
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@ast
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en-gb
type
label
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina)
@nl
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@ast
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en-gb
prefLabel
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina)
@nl
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@ast
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en-gb
P2093
P2860
P356
P1476
Role of HOXA7 to HOXA13 and PB ...... absence of uterus and vagina).
@en
P2093
Agnès Burel
Bertrand Knebelmann
Daniel Guerrier
Filiz Tiker
Isabelle Pellerin
Sylvie Odent
Thomas Mouchel
P2860
P2888
P356
10.1186/1477-5751-5-4
P407
P50
P577
2006-03-23T00:00:00Z
P5875
P6179
1002773324