Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens-Reference-Cited by-同舟云学术

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Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens

Published:2004-05 Issue:5 Volume:19 Page:1094-1100
ISSN:1460-2350
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Dayangaç Didem,Erdem Hayat,Yilmaz Engin,Şahin Ahmet,Sohn Christof,Özgüç Meral,Dörk Thilo

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynaecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/19/5/1094/17713596/deh223.pdf

Reference59 articles.

1. Anguiano A, Oates RD, Amos JA, Dean M, Gerrard B, Stewart C, Maher TA, White MB and Milunsky A (1992) Congenital bilateral absence of the vas deferens: a primarily genital form of cystic fibrosis. J Am Med Assoc267, 1794–1797.

2. Audrezet MP, Mercier B, Guillermit H, Quere I, Verlingue C, Rault G and Ferec C (1993) Identification of 12 novel mutations in the CFTR gene. Hum Mol Genet2, 51–54.

3. Augarten A, Yahav Y, Kerem BS, Halle D, Laufer J, Szeinberg A, Dor J, Mashiach S, Gazit E and Madgar I (1994) Congenital bilateral absence of the vas deferens in the absence of cystic fibrosis. Lancet344, 1473–1474.

4. Beaudet AL and Tsui L‐C (1993) A suggested nomenclature for designating mutations. Hum Mutat2, 245–248.

5. Bienvenu T, Beldjord C, Chelly J, Fonknechten N, Hubert D, Dusser D and Kaplan JC (1996) Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patients. Eur J Hum Genet4, 127–134.

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