Prenatal diagnosis of fukuyama type congenital muscular dystrophy in eight Japanese families by haplotype analysis using new markers closest to the gene

American Journal of Medical Genetics

Volumn 77, Issue 4, 1998, Pages 310-316

  Saito, Kayoko ^a   Kondo Iida, Eri ^a   Kawakita, Yukiko ^a   Juan, Du ^a   Ikeya, Kiyoko ^a   Osawa, Makiko ^a   Fukuyama, Yukio ^a   Toda, Tatsushi ^b   Nakabayashi, Masao ^a   Yamamoto, Tomoko ^a   Kobayashi, Makio ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

Ancestral founder allele; Cortical dysplasia; Fukuyama type congenital muscular dystrophy (FCMD); Haplotype analysis; Prenatal diagnosis

Indexed keywords

ALLELE; ARTICLE; CLINICAL ARTICLE; GENE ASSIGNMENT; HAPLOTYPE; HUMAN; JAPAN; MUSCULAR DYSTROPHY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

BRAIN; CHROMOSOMES; FEMALE; HAPLOTYPES; HUMANS; JAPAN; MALE; MICROSATELLITE REPEATS; MUSCULAR DYSTROPHIES; PEDIGREE; PRENATAL DIAGNOSIS;

EID: 0032557727     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980526)77:4<310::AID-AJMG12>3.0.CO;2-L     Document Type: Article

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