Identification of New Susceptibility Regions for X;Y Translocations in Patients with Testicular Disorder of Sex Development
Author:
Publisher
S. Karger AG
Subject
Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism
Reference19 articles.
1. Identification and characterization of an Xp22.33;Yp11.2 translocation causing a triplication of several genes of the pseudoautosomal region 1 in an XX male patient with severe systemic lupus erythematosus
2. The etiology of maleness in XX men
3. Complex mosaicism in sex reversed SRY+ male twins
4. Autosomal XX sex reversal caused by duplication ofSOX9
5. A selective difference between human Y-chromosomal DNA haplotypes
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1. Genetic Defects of Female Sexual Differentiation;Hormones, Brain and Behavior;2017
2. PRKX, a Novel cAMP-Dependent Protein Kinase Member, Plays an Important Role in Development;Journal of Cellular Biochemistry;2016-01-20
3. Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive;BMC Urology;2014-08-28
4. Unique Karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian Patient with Ovotesticular Disorder of Sexual Development;Sexual Development;2013
5. Sex chromosome aneuploidies among men with systemic lupus erythematosus;Journal of Autoimmunity;2012-05
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