Chromosome Abnormalities and Yq Microdeletions in Infertile Italian Couples Referred for Assisted Reproductive Technique
Author:
Publisher
S. Karger AG
Subject
Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism
Reference27 articles.
1. Ultrastructural studies of spermatozoa from infertile males with Robertsonian translocations and 18, X, Y aneuploidies
2. An excess of chromosome 1 breakpoints in male infertility
3. Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques
4. Segregation of a supernumerary del(15) marker chromosome in sperm
5. Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases
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1. Le caryotype avant ICSI, une procédure à abandonner ? Étude de pratiques au centre d’AMP du CHRU de Nancy;Gynécologie Obstétrique Fertilité & Sénologie ;2022-04
2. The Role of Genetic Mutations in Y Chromosome Infertility Syndrome;Annals of International clinical and medical Case Reports;2020-11-12
3. Evaluation of cytogenetic and y chromosome microdeletion analyzes in infertile cases;Meta Gene;2019-02
4. Homologous Robertsonian Translocations: Spectrum, Sex Ratios, and Reproductive Risks;Russian Journal of Genetics;2019-01
5. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions;Taiwanese Journal of Obstetrics and Gynecology;2017-06
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