Compound genetic abnormalities in patients with cystic fibrosis transmembrane regulator gene mutation
- 30 June 2007
- journal article
- case report
- Published by Elsevier in Fertility and Sterility
- Vol. 87 (6) , 1468.e5-1468.e8
- https://doi.org/10.1016/j.fertnstert.2006.07.1537
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regionsHuman Reproduction, 2003
- ACOG Technology Assessment in Obstetrics and Gynecology. Number 1, July 2002. Genetics and molecular diagnostic testingPublished by Wolters Kluwer Health ,2002
- Genetic risk factors in infertile men with severe oligozoospermia and azoospermia.Human Reproduction, 2002
- Impaired spermatogenesis in men with congenital absence of the vas deferensHuman Reproduction, 2001
- Compound genetic factors as a cause of male infertility: Case ReportHuman Reproduction, 2000
- Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia.JAMA, 1999
- Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosisPublished by American Medical Association (AMA) ,1992
- The Prognosis of Male Subferility: a Survey of 1025 Men Referred to a Fertility ClinicBritish Journal of Urology, 1984
- Frequency of azoospermiaForensic Science International, 1982
- Reproductive Failure in Males with Cystic FibrosisNew England Journal of Medicine, 1968