Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens-Reference-Cited by-同舟云学术

Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens

Published:2004-11-01 Issue:11 Volume:19 Page:2502-2508
ISSN:1460-2350
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Grangeia Ana,Niel Florence,Carvalho Filipa,Fernandes Susana,Ardalan Azarnouche,Girodon Emmanuelle,Silva Joaquina,Ferrás Luis,Sousa Mário,Barros Alberto

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynaecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/19/11/2502/6952653/deh462.pdf

Reference43 articles.

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2. 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.

3. Bernardino ALF, Lima CE and Zatz M (2003) Analysis of mutations in the cystic fibrosis transmembrane regulator (CFTR) gene in patients with obstructive azoospermia. Genet Mol Biol26, 1–3.

4. Boucher D, Creveaux I, Grizard G, Jimenez C, Hermabessière J and Dastugue B (1999) Screening for cystic fibrosis transmembrane conductance regulator gene mutations in men included in an intracytoplasmic sperm injection programme. Mol Hum Reprod5, 587–593.

5. Casals T, Bassas L, Egozcue S, Ramos MD, Giménez J, Segura A, Garcia F, Carrera M, Larriba S, Sarquella J and Estivill X (2000) Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens. Hum Reprod15, 1476–1483.

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