Congenital bilateral aplasia of vas deferens

Known as: Absent Vasa, Congenital Bilateral Aplasia of the Vas Deferens, Congenital Aplasia of Vas Deferens 
An autosomal recessive disorder that is associated with mutation(s) in the CFTR gene, encoding cystic fibrosis transmembrane conductance regulator… (More)
National Institutes of Health

Papers overview

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2004
2004
BACKGROUND Mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) can cause congenital bilateral absence of… (More)
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Highly Cited
2000
Highly Cited
2000
We have collated the results of cystic fibrosis (CF) mutation analysis conducted in 19 laboratories in France. We have analyzed 7… (More)
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Highly Cited
1997
Highly Cited
1997
Congenital absence of the vas deferens (CAVD) is a frequent cause for obstructive azoospermia and accounts for 1%–2% of male… (More)
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Review
1996
Review
1996
The condition of congenital bilateral absence of the vas deferens (CBAVD) is, in the majority of patients, related to defects in… (More)
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Highly Cited
1995
Highly Cited
1995
BACKGROUND Congenital bilateral absence of the vas deferens (CBAVD) is a form of male infertility in which mutations in the… (More)
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1995
1995
Congenital bilateral aplasia of the vas deferens (CBAVD) was suggested to be a mild form of cystic fibrosis (CF). Mutation… (More)
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Highly Cited
1995
Highly Cited
1995
Isolated congenital bilateral absence of the vas deferens (CBAVD) is an autosomal recessive disorder which has recently been… (More)
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1994
1994
The high frequency of mutations in the cystic fibrosis gene in patients with congenital bilateral absence of vas deferens (CBAVD… (More)
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1994
1994
Several recent studies have demonstrated the presence of mutations in the cystic fibrosis transmembrane conductance regulator… (More)
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Highly Cited
1992
Highly Cited
1992
OBJECTIVE Almost all males with cystic fibrosis (CF) have absent vasa deferentia. It has been suggested that otherwise healthy… (More)
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