The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches - Wikidata - wikimedia - TriplyDB

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches

http://www.wikidata.org/entity/Q25255341

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Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).Experimental uterus transplantation Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report.Uterus transplantation in the baboon: methodology and long-term function after auto-transplantation.Undiagnosed Hirsutism Associated Mayer-Rokitansky-Küster-Hauser Syndrome in Dermatology OPD.Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients Mayer-rokitansky-kuster-hauser syndrome: surgical management of two cases.Mayer-Rokitansky-Küster-Hauser syndrome Clinical approach for the classification of congenital uterine malformations Malformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH).Mayer-rokitansky-kuster-hauser syndrome: embryology, genetics and clinical and surgical treatment.MURCS Association with Partial Duplication of the Distal Long Chromosome 5 and Unilateral Ovarian Agenesis.Mayer-Rokitansky-Kuster-Hauser Type-B Anomaly with MURCS Association and Gonadal Dysgenesis.A Rare Case of Mayer-Rokitansky-Kuster-Hauser Syndrome Presenting with Acute Psychosis.Vaginal Agenesis in Mayer Rokitansky Kuster Hauser Syndrome.Uterine conserving surgery in a case of cervicovaginal agenesis with unicornuate uterus.Novel associations in disorders of sex development: findings from the I-DSD Registry.Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina.An assessment of the quality of the I-DSD and the I-CAH registries - international registries for rare conditions affecting sex development Diagnosis and laparoscopic management of a rudimentary uterine horn in a teenage girl, presenting with haematometra and severe endometriosis: our experience and review of literature.Uterine transplantation: a promising surrogate to surrogacy?Malformation syndromes associated with disorders of sex development.Report and review of described associations of Mayer-Rokitansky-Küster-Hauser syndrome and Silver-Russell syndrome.Recreation and procreation: A critical view of sex in the human female.Gestational surrogacy and the role of routine embryo screening: Current challenges and future directions for preimplantation genetic testing.Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.Mullerian dysgenesis: a critical review of the literature.The clinical application of laparoscope-assisted peritoneal vaginoplasty for the treatment of congenital absence of vagina.Selecting barrenness: the use of preimplantation genetic diagnosis by congenitally infertile women to select for infertility.Two sisters with Mayer-Rokitansky-Küster-Hauser syndrome and serous adenocarcinoma of the ovary.Mayer-Rokitansky-Kuster-Hauser syndrome with type 3 von Willebrand's disease: a case report and review of literature.ARCS/AUCS: A rare clinicoradiological presentation.Spectrum of MRI Appearance of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome in Primary Amenorrhea Patients.SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.MURCS and VACTERL association in a 27 year old female.Discordant Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome in identical twins - a case report and implications for reproduction in MRKH women.Molecular and Cellular Pathogenesis of Endometriosis.

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The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches

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2006 nî lūn-bûn

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2006 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2006年の論文

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The Mayer-Rokitansky-Küster-Ha ...... tations and genetic approaches

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Journal of Negative Results in BioMedicine

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Isabelle Pellerin

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Laurent Pasquier

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Thomas Mouchel

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A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman

Mutation of HOXA13 in hand-foot-genital syndrome

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome

Sexually dimorphic sterility phenotypes in Hoxa10-deficient mice

Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton

A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome

Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus

Requirement of Bmpr1a for Müllerian duct regression during male sexual development

Female development in mammals is regulated by Wnt-4 signalling

Wnt signaling in oncogenesis and embryogenesis--a look outside the nucleus

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perinatal disease

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