Novel mutations in the IRF6 gene for Van der Woude syndrome

Human Genetics

Volumn 113, Issue 5, 2003, Pages 382-386

  Wang, Xiaofang ^a,b   Liu, Jiali ^a,b   Zhang, Haibing ^a   Xiao, Mingzhen ^b   Li, Jinfeng ^c   Yang, Chunling ^d   Lin, Xianjun ^e   Wu, Zizhong ^e   Hu, Landian ^a   Kong, Xiangyin ^a  

^a Shanghai Jiao Tong University Affiliated Sixth People s Hospital   (China)

^b FOURTH MILITARY MEDICAL UNIVERSITY   (China)

^c XI'AN JIAOTONG UNIVERSITY   (China)

^d First Hospital of Quanzhou   (China)

^e The 88th Hospital of PLA   (China)

Author keywords

[No Author keywords available]

Indexed keywords

INTERFERON REGULATORY FACTOR 6; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; CHINESE; CLEFT LIP FACE PALATE; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; CRANIOFACIAL MALFORMATION; DNA FLANKING REGION; EXON; FAMILY STUDY; FEMALE; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NONSENSE MUTATION; PRIORITY JOURNAL; SCREENING TEST; SEQUENCE ANALYSIS; SPLICEOSOME; VAN DER WOUDE SYNDROME;

BASE SEQUENCE; CHINA; CHROMOSOME MAPPING; CLEFT LIP; CLEFT PALATE; CODON; CODON, NONSENSE; DNA-BINDING PROTEINS; FEMALE; HUMANS; INTERFERON REGULATORY FACTORS; MALE; MUTATION; MUTATION, MISSENSE; PEDIGREE; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0141989968     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-003-0989-2     Document Type: Article

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