Showing results (11-20 of 46) with videos related to
Sort By:
Pageof 5
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 1, 2023
Genetic Variants in SRD5A2 in a Spectrum of DSD Patients from Australian Clinics Highlight Importance of Genetic Testing alongside Typical First-Line InvestigationsGorjana Robevska, Chloe Hanna, Jocelyn van den Bergen, et al.Journal of the Endocrine Society|April 10, 2019
Functional Characterization of Two New Variants in the Bone Morphogenetic Protein 7 Prodomain in Two Pairs of Monozygotic Twins With HypospadiasAurore Bouty, Kelly Walton, Nurin Aisyiyah Listyasari, et al.Cell & Bioscience|January 4, 2024
COUP-TFII regulates early bipotential gonad signaling and commitment to ovarian progenitorsLucas G A Ferreira, Marina M L Kizys, Gabriel A C Gama, et al.Molecular and Cellular Endocrinology|January 20, 2022
Whole exome sequencing reveals copy number variants in individuals with disorders of sex developmentRajini Sreenivasan, Katrina Bell, Jocelyn van den Bergen, et al.Human Mutation|March 30, 2019
TP63-truncating variants cause isolated premature ovarian insufficiencyElena J Tucker, Sylvie Jaillard, Sonia R Grover, et al.International Journal of Pediatric Endocrinology|March 7, 2018
A novel, homozygous mutation in desert hedgehog (DHH) in a 46, XY patient with dysgenetic testes presenting with primary amenorrhoea: a case reportKaren M Rothacker, Katie L Ayers, Dave Tang, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 4, 2018
Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic ApproachesBrendan Backhouse, Chloe Hanna, Gorjana Robevska, et al.Stem Cell Reports|November 20, 2020
An In Vitro Differentiation Protocol for Human Embryonic Bipotential Gonad and Testis Cell DevelopmentIngrid M Knarston, Svenja Pachernegg, Gorjana Robevska, et al.Maturitas|July 1, 2026
MSH4 and MSH5 variants in premature ovarian insufficiency: A literature review and case studyJaidah Fergus-Mackie, Brianna L Kline, Gorjana Robevska, et al.Human Mutation|October 24, 2018
NR5A1 gene variants repress the ovarian-specific WNT signaling pathway in 46,XX disorders of sex development patientsIngrid M Knarston, Gorjana Robevska, Jocelyn A van den Bergen, et al.Pageof 5