SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 1, 1997, Pages 23-29

Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16

(6) Au, Kit Sing a Rodriguez, Joseph A a Rodriguez Jr , Estanislado a Dobyns, William B b Delgado, Mauricio R c Northrup, Hope a

a UNIVERSITY OF TEXAS MEDICAL SCHOOL (United States)

b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL (United States)

c UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER (United States)

Author keywords

deletions; mutations; polymorphisms; TSC2; tuberous sclerosis complex

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 16P; DNA SEQUENCE; GENE DELETION; GENE MUTATION; GENETIC LINKAGE; GENETIC POLYMORPHISM; HAMARTOMA; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; TUBEROUS SCLEROSIS;

BLOTTING, SOUTHERN; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POLYMORPHISM, GENETIC; TUBEROUS SCLEROSIS;

EID: 0031021317 PISSN: 10597794 EISSN: None Source Type: Journal
DOI: 10.1002/(SICI)1098-1004(1997)9:1<23::AID-HUMU4>3.0.CO;2-Q Document Type: Article

Times cited : (35)

References (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.