The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men-Reference-Cited by-同舟云学术

The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men

Published:2022-08-18 Issue:4 Volume:45 Page:519-529
ISSN:1976-9571
Container-title:Genes & Genomics
language:en
Short-container-title:Genes Genom

Author:

Jafari Leyla,Safinejad Kyumars^ORCID,Nasiri Mahboobeh,Heidari Mansour,Houshmand Massoud

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://link.springer.com/content/pdf/10.1007/s13258-022-01300-6.pdf

Reference34 articles.

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3. Asatiani K, Von Eckardstein S, Simoni M, Gromoll J, Nieschlag E (2003) CAG repeat length in the androgen receptor gene affects the risk of male infertility. Int J Androl 26:255–261

4. Balkan M, Tekes S, Gedik A (2008) Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey. J Assist Reprod Genet 25:559–565

5. Bourrouillou G, Dastugue N, Colomies P (1985) Chromosome studies in 952 infertile males with a sperm count below 10 million/ml. Hum Genet 71:366–367

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