Frequent missense mutations of fibroblast growth factor receptor (FGFR) gene families in craniofacial syndromes in Japanese patients

Rinsho byori. The Japanese journal of clinical pathology

Volumn 44, Issue 5, 1996, Pages 439-443

  Ishigaki, M ^a   Wada, C ^a   Toyo oka, Y ^a   Yamabe, H ^a   Ohnuki, Y ^a   Takada, F ^a   Yamazaki, Y ^a   Ohtani, H ^a  

^a KITASATO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ARTICLE; CONGENITAL MALFORMATION; FACIAL BONE; GENETICS; HUMAN; JAPAN; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; SKULL; SYNDROME;

BASE SEQUENCE; FACIAL BONES; HUMANS; JAPAN; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RECEPTORS, FIBROBLAST GROWTH FACTOR; SKULL; SYNDROME;

EID: 0030139689     PISSN: 00471860     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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