Molecular diagnosis of congential bilateral absence of the vas deferens: Analyses of the CFTR gene in 64 French patients

Annales de Genetique

Volumn 40, Issue 1, 1997, Pages 5-9

  Bienvenu, T ^a   Adjiman, M ^a   Thiounn, N ^a   Jeanpierre, M ^a   Hubert, D ^a   Lepercq, J ^a   Francoual, C ^a   Wolf, J Ph ^a   Izard, V ^a   Jouannet, P ^a   Kaplan, J C ^a   Beldjord, C ^a  

^a Hopital Cochin ^*  (France)

Author keywords

Congenital bilateral absence of the vas deferens; Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator

Indexed keywords

MESSENGER RNA; TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR PROTEIN, HUMAN;

AGENESIS; ALLELE; ARTICLE; CODON; DNA FLANKING REGION; FERTILIZATION IN VITRO; GENE MUTATION; GENETIC COUNSELING; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; VAS DEFERENS; CONGENITAL MALFORMATION; ELECTROPHORESIS; FRANCE; GENETICS; GENOTYPE; INTRON; METHODOLOGY; MUTATION; OLIGOSPERMIA; PATHOLOGY;

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; ELECTROPHORESIS; FRANCE; GENOTYPE; HUMANS; INTRONS; MALE; MUTATION; OLIGOSPERMIA; VAS DEFERENS;

EID: 0030609943     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (24)