scholarly journals Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens

1996 ◽  
Vol 52 (2) ◽  
pp. 225-225
Keyword(s):  
Cystic Fibrosis ◽  
Vas Deferens ◽  
Congenital Absence ◽  
Cystic Fibrosis Gene

CONGENITAL ABSENCE OF THE VAS DEFERENS: INCOMPLETE PENETRANCE OF CYSTIC FIBROSIS GENE MUTATIONS

1997 ◽  
Vol 158 (5) ◽  
pp. 1794-1799 ◽  
Author(s):  
David Shin ◽  
Fred Gilbert ◽  
Marc Goldstein ◽  
Peter N. Schlegel
Keyword(s):  
Cystic Fibrosis ◽  
Vas Deferens ◽  
Gene Mutations ◽  
Congenital Absence ◽  
Cystic Fibrosis Gene ◽  
Incomplete Penetrance

Novel Missense Mutations in the Cystic Fibrosis Gene of Brazilian Patients With Congenital Absence of Vas Deferens

2005 ◽  
Vol 84 ◽  
pp. S223-S224
Author(s):  
P.C. Pieri ◽  
M.T. Missaglia ◽  
J.A. Roque ◽  
C.A. Moreira-Filho ◽  
J. Hallak
Keyword(s):  
Cystic Fibrosis ◽  
Vas Deferens ◽  
Congenital Absence ◽  
Cystic Fibrosis Gene ◽  
Missense Mutations

scholarly journals Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

1995 ◽  
Vol 332 (22) ◽  
pp. 1475-1480 ◽  
Author(s):  
Miguel Chillón ◽  
Teresa Casals ◽  
Bernard Mercier ◽  
Lluís Bassas ◽  
Willy Lissens ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Vas Deferens ◽  
Congenital Absence ◽  
Cystic Fibrosis Gene

scholarly journals R-096. Cystic fibrosis gene mutations do not affect ICSI outcome in men with congenital absence of the vas deferens

1997 ◽  
Vol 12 (Suppl_2) ◽  
pp. 277-278
Author(s):  
J.L.I. Romero ◽  
Y. Mínguez ◽  
C. Rubio ◽  
A. Ruiz ◽  
M.D. Molero ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Vas Deferens ◽  
Gene Mutations ◽  
Congenital Absence ◽  
Cystic Fibrosis Gene

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

2000 ◽  
Vol 16 (2) ◽  
pp. 143-156 ◽  
Author(s):  
Mireille Claustres ◽  
Caroline Guittard ◽  
Dominique Bozon ◽  
Fran�oise Chevalier ◽  
Claudine Verlingue ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Vas Deferens ◽  
Congenital Absence ◽  
Cftr Mutations
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