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Volumn 104, Issue 2, 2001, Pages 152-156

Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter

(5) Tanamy, Meital Gal a Magal, Nurit a Halpern, Gabrielle J a Jaber, Lutfi b,c Shohat, Mordechai a,c

a RABIN MEDICAL CENTER (Israel)

b SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL (Israel)

c TEL AVIV UNIVERSITY (Israel)

Author keywords

Arthrogryposis multiplex congenita; Homozygosity; Markers

Indexed keywords

ARTHROGRYPOSIS; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 5Q; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL MEDICINE; CONTROLLED STUDY; DISEASE CLASSIFICATION; GENE MAPPING; GENETIC MARKER; HAPLOTYPE; HOMOZYGOSITY; HUMAN; JOINT CONTRACTURE; PRIORITY JOURNAL;

ALLELES; ARTHROGRYPOSIS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; EXPRESSED SEQUENCE TAGS; GENETIC MARKERS; HAPLOTYPES; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MICROSATELLITE REPEATS; MODELS, GENETIC; MUTATION; PHYSICAL CHROMOSOME MAPPING; RECOMBINATION, GENETIC;

EID: 0035935634 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10030 Document Type: Article

Times cited : (14)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.