Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France. [electronic resource]
Producer: 20000919Description: 143-56 p. digitalISSN:- 1059-7794
- Adult
- Alleles
- Chromosome Deletion
- Cystic Fibrosis -- epidemiology
- Cystic Fibrosis Transmembrane Conductance Regulator -- genetics
- Frameshift Mutation -- genetics
- France -- epidemiology
- Gene Frequency
- Genotype
- Humans
- Infertility, Male -- epidemiology
- Male
- Middle Aged
- Mutagenesis, Insertional -- genetics
- Mutation -- genetics
- Mutation, Missense -- genetics
- Polymorphism, Genetic -- genetics
- Vas Deferens -- abnormalities
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Publication Type: Comparative Study; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
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