Y chromosome microdeletions and alterations of spermatogenesis, patient approach and genetic counseling
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Reference19 articles.
1. International estimates of infertility prevalence and treatment-seeking: potential need and demand for infertility medical care;Boivin;Hum Reprod,2007
2. The genetic causes of male factor infertility: a review;O’Flynn O’Brien;Fertil Steril,2010
3. A comprehensive review of genetics and genetic testing in azoospermia;Hamada;Clinics,2013
4. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm;Tiepolo;Hum Genet,1976
5. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11;Vogt;Hum Mol Genet,1996
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1. Stratégies de prise en charge des azoospermies non obstructives relevant d’une atteinte testiculaire primitive;Bulletin de l'Académie Nationale de Médecine;2022-12
2. Establishment of human embryonic stem cell (SKLRMe001-A)carrying Azoospermic factor c (AZFc) deletions;Stem Cell Research;2022-03
3. Immunogenetic causes of infertility;A Molecular Approach to Immunogenetics;2022
4. Pathogenic variants of ATG4D in infertile men with non‐obstructive azoospermia identified using whole‐exome sequencing;Clinical Genetics;2021-06-11
5. The infertile male patient with a genetic cause;Assisted Reproduction Techniques;2021-06-04
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