Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens
Author:
Publisher
Oxford University Press (OUP)
Subject
Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine
Link
http://academic.oup.com/humrep/article-pdf/24/3/748/1805865/den413.pdf
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3. High-Resolution Global Profiling of Genomic Alterations with Long Oligonucleotide Microarray
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5. Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens
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1. Heterogeneous spectrum of CFTR gene mutations in Chinese patients with CAVD and the dilemma of genetic blocking strategy;Reproduction;2022-09-01
2. Congenital Bilateral Absence of the Vas Deferens;Frontiers in Genetics;2022-02-11
3. Copy Number Variation Analysis in Turkish Patients with Congenital Bilateral Absence of Vas Deferens;Acta Medica Alanya;2021-08-01
4. A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens;Journal of Assisted Reproduction and Genetics;2020-04-20
5. Genetics of the congenital absence of the vas deferens;Human Genetics;2020-02-05
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