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Volumn 43, Issue 2, 2006, Pages 142-147

Q289P mutation in FGFR2 gene causes saethre-chotzen syndrome: Some considerations about familial heterogeneity

Author keywords

Acrocephalosyndactyly; Craniosynostosis; Crouzon syndrome; FGFR2; Saethre Chotzen Syndrome

Indexed keywords

ACROCEPHALOSYNDACTYLY; ALLELISM; ARTICLE; CLINICAL ARTICLE; CONGENITAL DISORDER; CROUZON SYNDROME; EXON; FAMILIAL DISEASE; FGFR2 GENE; GENE; GENE INTERACTION; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC SCREENING; HUMAN; JACKSON WEISS SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TERATOLOGY; TWIST GENE ANALYSIS;

EID: 33644999811     PISSN: 10556656     EISSN: None     Source Type: Journal    
DOI: 10.1597/04-155.1     Document Type: Article
Times cited : (17)

References (25)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.