Testicular Expressed Genes Are Missing in Familial X-Linked Kallmann Syndrome due to Two Large Different Deletions in Daughter’s X Chromosomes
Author:
Publisher
S. Karger AG
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
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1. Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure;The American Journal of Human Genetics;2022-08
2. Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism;The Journal of Clinical Endocrinology & Metabolism;2022-05-16
3. Novel interstitial deletion in Xp22.3 in a typical X-linked recessive family with Kallmann syndrome;Andrologia;2018-02-14
4. Xp22.31 Microdeletion due to Microhomology-Mediated Break-Induced Replication in a Boy with Contiguous Gene Deletion Syndrome;Cytogenetic and Genome Research;2017
5. Testosterone and Male Infertility;Urologic Clinics of North America;2016-05
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