Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms

American Journal of Human Genetics

Volumn 49, Issue 5, 1991, Pages 951-960

  Clemens, P R ^a   Fenwick, R G ^a   Chamberlain, J S ^a   Gibbs, R A ^a   De Andrade, M ^a   Chakraborty, R ^a   Caskey, C T ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; OLIGONUCLEOTIDE; PRIMER DNA;

ARTICLE; BECKER MUSCULAR DYSTROPHY; CLINICAL ARTICLE; DNA SEQUENCE; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE FREQUENCY; HETEROZYGOTE DETECTION; HUMAN; MALE; NORMAL HUMAN; PEDIGREE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ALLELES; BASE SEQUENCE; CELLS, CULTURED; DYSTROPHIN; FEMALE; GENE FREQUENCY; GENETIC MARKERS; HETEROZYGOTE DETECTION; HUMAN; MALE; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHIES; PEDIGREE; POLYDEOXYRIBONUCLEOTIDES; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); PREGNANCY; PRENATAL DIAGNOSIS; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

DIPLEX;

EID: 0025943652     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)