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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 2010
A serotonin and melanocortin circuit mediates D-fenfluramine anorexiaYong Xu, Juli E Jones, Danielle A Lauzon, et al.Journal of Pediatric Urology|May 4, 2007
DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13Nilda M Garcia, Jocelyn Allgood, Lane J Santos, et al.American Journal of Medical Genetics. Part A|August 7, 2013
Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failureSteven M Harrison, Ian M Campbell, Melise Keays, et al.Human Reproduction (Oxford, England)|October 26, 2007
Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrheaTeresa D Gallardo, George B John, Karen Bradshaw, et al.Journal of Human Genetics|September 9, 2016
Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot regionSara Benito-Sanz, Alberta Belinchon-Martínez, Miriam Aza-Carmona, et al.European Journal of Human Genetics : EJHG|March 4, 2011
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral developmentElizabeth J Bhoj, Purita Ramos, Linda A Baker, et al.Human Genetics|April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesLane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.Proceedings of the National Academy of Sciences of the United States of America|June 28, 2018
Sex-chromosome dosage effects on gene expression in humansArmin Raznahan, Neelroop N Parikshak, Vijay Chandran, et al.JCI Insight|November 2, 2019
NK cell defects in X-linked pigmentary reticulate disorderPetro Starokadomskyy, Katelynn M Wilton, Konrad Krzewski, et al.American Journal of Medical Genetics. Part A|November 26, 2010
UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patientsNicole de Leeuw, Saskia Bulk, Andrew Green, et al.Pageof 5