The Genetic Basis of Congenital Bilateral Absence of the Vas Deferens and Cystic Fibrosis
- 2 January 1994
- journal article
- review article
- Published by Wiley in Journal of Andrology
- Vol. 15 (1) , 1-8
- https://doi.org/10.1002/j.1939-4640.1994.tb01672.x
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Cystic fibrosis: molecular biology and therapeutic implicationsScience, 1992
- Microscopic epididymal sperm aspiration (MESA): A new option for treatment of the obstructive azoospermia associated with cystic fibrosisJournal of Assisted Reproduction and Genetics, 1992
- Vasa Aplasia and Cystic FibrosisBritish Journal of Urology, 1990
- A morphological study of the efferent ducts of the human epididymisInternational Journal of Andrology, 1990
- Abnormal distribution of CF ΔF508 allele in azoospermic men with congenital aplasia of epididymis and vas deferensThe Lancet, 1990
- Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patientsCell, 1990
- Mutation Analysis for Heterozygote Detection and the Prenatal Diagnosis of Cystic FibrosisNew England Journal of Medicine, 1990
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989
- OBSTRUCTIVE AZOOSPERMIA AS A DIAGNOSTIC CRITERION FOR THE CYSTIC FIBROSIS SYNDROMEThe Lancet, 1982
- Congenital mesonephric defects in male infants with mucoviscidosisJournal of Clinical Pathology, 1969