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Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeThe Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approachesThe genes for a spliceosome protein (SAP62) and the anti-Müllerian hormone (AMH) are contiguousA conserved non-homeodomain Hoxa9 isoform interacting with CBP is co-expressed with the 'typical' Hoxa9 protein during embryogenesisInducible expression of beta defensins by human respiratory epithelial cells exposed to Aspergillus fumigatus organisms.Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.Candidate Sertoli cell specific promoter element for a TGFbeta family member (Amh) and a 3' UTR enhancer/repressor for the same gene.Anti-müllerian hormone: the Jost factor.Involvement of ITIH5, a candidate gene for congenital uterovaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome), in female genital tract development.In vivo analysis of the regulation of the anti-Müllerian hormone, as a marker of Sertoli cell differentiation during testicular development, reveals a multi-step process.[Molecular biology of normal and pathologic anti-müllerian hormone]Mapping of the gene for anti-müllerian hormone to the short arm of human chromosome 19GATA-1 is a potential repressor of anti-Müllerian hormone expression during the establishment of puberty in the mouse[The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and genetics][Response from K. Morcel to the article from A. El Khamlichi et al.: Typical form of Mayer-Rokitansky-Küster-Hauser syndrome and ectopic kidney. A rare association. Gynecol Obstet Fertil 2011;39:e40-e43]
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