AZFa Microdeletions: Occurrence in Chinese Infertile Men and Novel Deletions Revealed by Semiconductor Sequencing
Author:
Funder
Science and Technology Department of Jilin Province
Publisher
Elsevier BV
Subject
Urology
Reference30 articles.
1. Spermatogenesis in a man with complete deletion of USP9Y;Luddi;N Engl J Med,2009
2. Prevalent false positives of azoospermia factor a (AZFa) microdeletions caused by single-nucleotide polymorphism rs72609647 in the sY84 screening of male infertility;Wu;Asian J Androl,2011
3. Copy number variation in the human Y chromosome in the UK population;Wei;Hum Genet,2015
4. Novel Y-chromosomal microdeletions associated with non-obstructive azoospermia uncovered by high throughput sequencing of sequence-tagged sites (STSs);Liu;Sci Rep,2016
5. Male infertility in China: laboratory finding for AZF microdeletions and chromosomal abnormalities in infertile men from Northeastern China;Wang;J Assist Reprod Genet,2010
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1. Concomitance of 47,XXY, a balanced reciprocal translocation of t(4;17)(q12;q11.2) encompassing SPINK2 at 4q12 and NOS at 17q11.2 and an AZFa sY86 deletion in an infertile male;Taiwanese Journal of Obstetrics and Gynecology;2023-03
2. Repetitive DNA Sequences in the Human Y Chromosome and Male Infertility;Frontiers in Cell and Developmental Biology;2022-07-13
3. Investigation of genotype–phenotype correlation in patients with AZF microdeletion in a single‐reference centre;Andrologia;2021-07-11
4. Targeted next-generation sequencing panel screening of 668 Chinese patients with non-obstructive azoospermia;Journal of Assisted Reproduction and Genetics;2021-03-16
5. Y chromosome structural variation in infertile men detected by targeted next-generation sequencing;Journal of Assisted Reproduction and Genetics;2021-01-16
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