Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers

Human Mutation

Volumn 8, Issue 2, 1996, Pages 149-159

  Morral, Núria ^a,f   Dörk, Thilo ^b   Llevadot, Roser ^a   Dziadek, Violetta ^b   Mercier, Bernard ^c   Férec, Claude ^c   Costes, Bruno ^d   Girodon, Emmanuelle ^d   Zielenski, Julian ^e   Tsui, Lap Chee ^e   Tümmler, Burkhard ^b   Estivill, Xavier ^a  

^a Institut de Recerca Oncologica   (Spain)

^b HANNOVER MEDICAL SCHOOL   (Germany)

^c Ctr Transfus Sang de Biogenetique   (France)

^d INSERM   (France)

^e HOSPITAL FOR SICK CHILDREN   (Canada)

^f BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Cystic fibrosis; Haplotypes; Mutation screening

Indexed keywords

DNA; MICROSATELLITE DNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONTROLLED STUDY; CYSTIC FIBROSIS; GENE MUTATION; GENETIC MARKER; GENETIC POLYMORPHISM; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; POPULATION GENETICS; PRIORITY JOURNAL; REGULATOR GENE;

CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA; DNA, SATELLITE; GENETIC MARKERS; HAPLOTYPES; HUMANS; MUTATION; POLYMORPHISM, GENETIC;

EID: 15844373505     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1996)8:2<149::AID-HUMU7>3.0.CO;2-6     Document Type: Article

References (19)

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