SCOPUS 정보 검색 플랫폼

Volumn 37, Issue 10, 2000, Pages 785-787

The mutation spectrum in Holt-Oram syndrome [1]

(15) Cross, S J a Ching, Y H a Li, Q Y a Arsmtrong Buisseret, L a Spranger, S a Lyonnet, S a Bonnet, D a Penttinen, M a Jonveaux, P a Leheup, B a Mortier, G a Van Ravenswaaij, C a Gardiner, C A a Brook, J D a Newbury Ecob, R a

a UNIVERSITY OF NOTTINGHAM (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; TRANSCRIPTION FACTOR;

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12Q; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CPG ISLAND; DEVELOPMENTAL DISORDER; FORELIMB; GENE MUTATION; HOLT ORAM SYNDROME; HUMAN; LETTER; LIMB MALFORMATION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; TUMOR SUPPRESSOR GENE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENETIC SCREENING; GENOTYPE; HEART BLOCK; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS; HUMAN; INTRONS; LIMB DEFORMITIES, CONGENITAL; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SYNDACTYLY; SYNDROME; VARIATION (GENETICS);

EID: 0033788894 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (61)

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10
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11
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13
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- Contact Dr Gareth Cross; gcrossνcht.org.uk

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.