SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 3, 1996, Pages 613-619

A second locus for Rieger syndrome maps to chromosome 13q14

(7) Phillips, Jeffrey C a,b Del Bono, Elizabeth A a Haines, Jonathan L c Pralea, Anca Madalina a Cohen, John S e Greff, Linda J e Wiggs, Janey L a,b,d

a TUFTS MEDICAL CENTER (United States)

b TUFTS UNIVERSITY (United States)

c MASSACHUSETTS GENERAL HOSPITAL (United States)

d TUFTS UNIVERSITY SCHOOL OF MEDICINE (United States)

e CINCINNATI EYE INSTITUTE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLINDNESS; CHROMOSOME 13Q; CHROMOSOME 4Q; CHROMOSOME MAP; CONGENITAL MALFORMATION; GENE LOCUS; GENETIC LINKAGE; GLAUCOMA; HUMAN; HUMAN CELL; MORPHOGENESIS; PRIORITY JOURNAL; RIEGER SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; EYE ABNORMALITIES; EYE DISEASES, HEREDITARY; GENES, DOMINANT; GLAUCOMA; HUMANS; MALE; PEDIGREE; SYNDROME; TOOTH ABNORMALITIES; UMBILICUS;

UMBILICUS;

EID: 0029762015 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (173)

References (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.