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Prenatal Diagnosis|June 7, 2022
Prenatal detection and evaluation of differences of sex development: A qualitative interview study of parental perspectives and unmet needsJ Whitehead, Josephine Hirsch, Ilina Rosoklija, et al.Ophthalmic Genetics|April 6, 2022
Ocular findings in pediatric turner syndromeJonathan Huang, Syeda Sumara Taranum Basith, Sheetal Patel, et al.Journal of Pediatric Urology|May 10, 2025
Role of endocrine and genetic evaluation for infants with proximal hypospadiasVictoria S Lee, Courtney Finlayson, Josephine Hirsch, et al.Urology|June 2, 2024
Turner Syndrome With Y Chromosome and Germ Cells: A Case Report Highlighting the Need to Prioritize Individualized CareJennifer N Rosen, Courtney Finlayson, Jaclyn L Papadakis, et al.Frontiers in Urology|August 8, 2025
Comparison of web-based information about cell-free DNA prenatal screening: implications for differences of sex development careSoojin Kim, Esther L Finney, Ushasi Naha, et al.Pediatric Cardiology|October 9, 2023
Outcomes and Associated Extracardiac Malformations in Neonates from Colombia with Severe Congenital Heart DiseaseJorge L Alvarado, Anderson Bermon, Claudia Florez, et al.Ophthalmic Genetics|May 6, 2026
Evaluating gene-disease relationship strength in crystallin genes in association with pediatric cataractsAlexander Ing, Allison Goetsch Weisman, Andy Drackley, et al.Genes|August 28, 2025
<i>GPR143</i>-Associated Ocular Albinism in a Hispanic Family and Review of the LiteratureAnushree Aneja, Brenda L Bohnsack, Valerie Allegretti, et al.The Journal of Urology|July 5, 2024
Mixed Gonadal Dysgenesis: A Narrative Literature Review and Clinical Primer for the UrologistLauren E Corona, Victoria S Lee, Allison Goetsch Weisman, et al.Genes|May 4, 2026
A Case of Aymé-Gripp Syndromic Congenital Cataracts and Pigmentary Retinopathy Caused by a Novel MAF Variant in the N-Terminal Transactivation Domain-A Case Report and Literature ReviewMax Chauhan, Kaersti L Rickels, Sudhi P Kurup, et al.Pageof 3