SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 8, 2001, Pages 642-645

TP63 gene mutation in ADULT syndrome

(7) Amiel, Jeanne a Bougeard, Gaëlle b Francannet, Christine c Raclin, Valérie a Munnich, Arnold a Lyonnet, Stanislas a Frebourg, Thierry b

a HÔPITAL NECKER ENFANTS MALADES (France)

b INSERM (France)

c HÔTEL DIEU (France)

Author keywords

Adult syndrome; EEC syndrome; Limb abnormality; SHFM; TP63

Indexed keywords

ADULT SYNDROME; ARTICLE; CASE REPORT; CHROMOSOME 3Q; CHROMOSOME MAP; ECTODERMAL ECTRODACTYLY CLEFTING; ECTRODACTYLY; FEMALE; GENE LOCUS; HUMAN; LIMB MAMMARY SYNDROME; MISSENSE MUTATION; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; SPLIT HAND FOOT MALFORMATION;

ABNORMALITIES, MULTIPLE; ALLELES; CHILD; FEMALE; GENES, DOMINANT; GENOTYPE; HUMANS; LIMB DEFORMITIES, CONGENITAL; LINKAGE (GENETICS); MUTATION; NIPPLES; SYNDROME;

EID: 0034882201 PISSN: 10184813 EISSN: None Source Type: Journal
DOI: 10.1038/sj.ejhg.5200676 Document Type: Article

Times cited : (75)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.