Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study
about
TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasiaThe genetic basis of female reproductive disorders: etiology and clinical testingWnt4 coordinates directional cell migration and extension of the Müllerian duct essential for ontogenesis of the female reproductive tract.Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findingsApplication of the new classification on patients with a disorder of sex development in indonesia.Pax8 modulates the expression of Wnt4 that is necessary for the maintenance of the epithelial phenotype of thyroid cellsGenetic Syndromes and Genes Involved in the Development of the Female Reproductive Tract: A Possible Role for Gene Therapy.A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patientsMutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure.Gene expression profile of patients with Mayer-Rokitansky-Küster-Hauser syndrome: new insights into the potential role of developmental pathways.Evaluation of SHOX copy number variations in patients with Müllerian aplasia.Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.Building pathways for ovary organogenesis in the mouse embryo.Association of WNT4 polymorphisms with endometriosis in infertile patientsVertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literatureMayer-rokitansky-kuster-hauser syndrome: embryology, genetics and clinical and surgical treatment.WINGLESS (WNT) signaling is a progesterone target for rat uterine stromal cell proliferation.Molecular analysis of the beta-catenin gene in patients with the Mayer-Rokitansky-Küster-Hauser syndrome.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.Coexistence of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome in 46, XX female: A case report and review of literature.Acne and PCOS are less frequent in women with Mayer-Rokitansky-Küster-Hauser syndrome despite a high rate of hyperandrogenemia: a cross-sectional studyGene mutations associated with anomalies of human gonad formation.Mayer-Rokitansky-Kuster-Hauser syndrome: complications, diagnosis and possible treatment options: a review.Adrenocortical growth and cancer.The Battle of the Sexes: Human Sex Development and Its Disorders.Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.Mechanism of Sex Determination in Humans: Insights from Disorders of Sex Development.Mullerian dysgenesis: a critical review of the literature.Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype.Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development.Congenital Malformations of the Reproductive Tract in a Patient with Poland Syndrome: Is There a Connection?Hyperandrogenemia and ovarian reserve in patients with Mayer-Rokitansky-Küster-Hauser syndrome type 1 and 2: potential influences on ovarian stimulation.Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia.SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome.Etiologies of uterine malformations.Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome: a case report and review of the literature.
P2860
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P2860
Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study
description
2008 nî lūn-bûn
@nan
2008 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մարտին հրատարակված գիտական հոդված
@hy
2008年の論文
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2008年論文
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2008年論文
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2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
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name
Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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type
label
Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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Identification and functional ...... : a French collaborative study
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P2093
P50
P921
P3181
P356
P1476
Identification and functional ...... : a French collaborative study
@en
P2093
Anna Biason-Lauber
Catherine Pienkowski
Charles Sultan
Eugene Schoenle
Françoise Paris
P304
P3181
P356
10.1210/JC.2007-2023
P407
P577
2008-01-08T00:00:00Z