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WNT4 deficiency
Müllerian Aplasia and Hyperandrogenism
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Orphanet Report Series Rare Diseases Collection
Thesis Hsf 2018 Maison Patrick
Genetics, Underlying Pathologies and Psychosexual Differentiation Valerie A
Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome a Comprehensive Update Herlin, Morten Krogh; Petersen, Michael Bjørn; Brännström, Mats
Cell-Intrinsic Wnt4 Controls Early Cdc1 Commitment and Suppresses
Université De POITIERS Faculté De Médecine Et De Pharmacie THESE
From Gene to Gender - What We’Ve Learned and What We Need to Learn - New Prospects in DSD Research
Universidade De Brasília Instituto De Ciências Biológicas Programa De Pós Graduação Em Biologia Animal
Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome
'Control of Sex Development'
Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: a Comprehensive Update Morten Krogh Herlin1,2* , Michael Bjørn Petersen1,3 and Mats Brännström4
Analysis of Copy Number Variations Of
Genome-Wide Screening of Biomarkers in Androgen Insensitivity Syndrome (AIS)
Estrogen Regulation of Mtor Signaling and Mitochondrial Function in Invasive Lobular Carcinoma Cell Lines Requires WNT4
Mayer-Rokitansky-Kuster-Hauser Syndrome by Hannah
Apoptosis-Regulating Factors in Developing and Adult Ovaries
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WNT4 Gene Wnt Family Member 4
Bilateral Ovotestes in a Female Beagle Dog
WNT4 and Sex Development
Mayer-Rokitansky-Kuster-Hauser Syndrome: Embryology, Genetics and Clinical and Surgical Treatment
Mutation Analysis of the WNT4 Gene in Han Chinese Women With
Hyperandrogenemia and High Prolactin in Congenital Utero–Vaginal Aplasia Patients
Management of the Infant with Atypical Genitalia (Disorder of Sex Development)
A Case of Mayer-Rokitansky-Kuster-Hauser Syndrome
A Balanced Chromosomal Translocation
11B-Hydroxylase Deficiency, 36 17,20 Desmolase Deficiency, 36 17
Sex Determination and Disorders of Sex Development According to the Revised Nomenclature and Classification in 46,XX Individuals
Mechanisms in Disorders of Sex Development
Review Article Mayer-Rokitansky-Kuster-Hauser Syndrome: Embryology, Genetics and Clinical and Surgical Treatment
Atypical Case of Mayer–Rokitansky–Kuster–Hauser Syndrome and Amyloidosis: Is There a Link Or Association?
An Update on Genetics of Disorders of Sexual Development Along With
Role of Wnt4 Signaling in Mammalian Sex Determination, Ovariogenesis and Female Sex Duct Differentiation
8 Disorders of Sex Development: a New Definition and Classification