Author:
Chien Shu-Chin,Li Yueh-Chun,Ho Ming,Hsu Pei-Ching,Teng Ru-Hsiou,Lin Wei-De,Tsai Fuu-Jen,Lin Chyi-Chyang
Subject
Genetics (clinical),Genetics
Cited by
8 articles.
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1. The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation and Neuromuscular Pathology;Cytology and Genetics;2022-09-20
2. An azoospermic male with a novel chromosome 46,
XX
, der(15)t(Y; 15)(p11.3; p12);Clinical Case Reports;2022-07
3. A 46,XX karyotype in men with infertility: Two new cases and review of the literature;Journal of Human Reproductive Sciences;2022
4. Localization of the SRY Gene on Chromosome 3 in a Patient with Azoospermia and a Complex Karyotype 45,X/46,X,i(Y)(q10)/46,XX/ 47,XX,i(Y)(q10);Cytogenetic and Genome Research;2018
5. Sex Chromosomes, Sex Chromosome Disorders, and Disorders of Sex Development;The Principles of Clinical Cytogenetics;2012-08-30