Les génotypes responsables de mucoviscidose ou d’absence bilatérale des canaux déférents ABCD
Author:
Publisher
Springer Science and Business Media LLC
Subject
Urology,Reproductive Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF03034631.pdf
Reference38 articles.
1. AUGARTEN A., YAHAV Y., KEREM B.S. et al.: Congenital bilateral absence of vas deferens in the absence of cystic fibrosis [see comments]. Lancet., 1994, 344: 1473–1474.
2. BOUCHER D., CREVEAUX I., GRIZARD G., JIMENEZ C., HERMABESSIERE J., DASTUGUE B.: Screening for cystic fibrosis transmembrane conductance regulator gene mutations in men included in an intracytoplasmic sperm injection programme. Mol. Hum. Reprod., 1999, 5: 587–593.
3. CASALS T., BASSAS L., EGOZCUE S. et al.: Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens. Hum. Reprod., 2000, 15: 1476–1483.
4. CLAUSTRES M., GUITTARD C., BOZON D. et al.: Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France. Hum. Mutat., 2000, 16: 143–156.
5. CHILLON M., CASALS T., MERCIER B. et al.: Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N. Engl. J. Med., 1995, 332: 1475–1480.
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