Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis

European Journal of Human Genetics

Volumn 10, Issue 4, 2002, Pages 231-238

  Moutou, Céline ^a   Gardes, Nathalie ^a   Viville, Stéphane ^a  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

Cystic fibrosis, CF; Multiplex fluorescent PCR; Pre implantation genetic diagnosis, PGD

Indexed keywords

MICROSATELLITE DNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADULT; ALLELE; ARTICLE; BLASTOMERE; CLINICAL PROTOCOL; CONTROLLED STUDY; CYSTIC FIBROSIS; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DNA POLYMORPHISM; FEMALE; FETUS; FLUORESCENCE; GENE IDENTIFICATION; GENE MUTATION; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; LYMPHOBLAST; MALE; MEIOSIS; MICROSATELLITE MARKER; NONHUMAN; PEDIGREE ANALYSIS; PLOIDY; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; SAFETY; SIGNAL TRANSDUCTION;

EID: 0036078234     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200794     Document Type: Article

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