A rare case of 46, XX (SRY positive) testicular disorder of sex development with growth hormone deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference20 articles.
1. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif;Sinclair;Nature,1990
2. Rare case of monocentric isochromosome Y with inversion duplication of p arm in patient diagnosed with azoospermia;Aftab;Andrologia,2020
3. The crucial role of SRY gene in the determination of human genetic sex: 46, XX disorder of sex development;Albu;Rom J Morphol Embryol,2019
4. Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive;Wu;BMC Urol,2014
5. Disorders of sex development with testicular differentiation in SRY-Negative 46, XX individuals: clinical and genetic aspects;Grinspon;Sex Dev,2016
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Non-Invasive Prenatal Test Analysis Opens a Pandora’s Box: Identification of Very Rare Cases of SRY-Positive Healthy Females, Segregating for Three Generations Thanks to Preferential Inactivation of the XqYp Translocated Chromosome;Genes;2024-01-16
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