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Volumn 16, Issue 5, 2005, Pages 851-856
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Identification of novel mutations of IRF6 gene in Chinese families with Van der Woude syndrome.
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Author keywords
[No Author keywords available]
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Indexed keywords
INTERFERON REGULATORY FACTOR;
IRF6 PROTEIN, HUMAN;
ARTICLE;
ASIAN;
CLEFT LIP;
CLEFT PALATE;
CRANIOFACIAL MALFORMATION;
EXON;
GENETIC LINKAGE;
GENETICS;
HUMAN;
HYPODONTIA;
MUTATION;
NUCLEOTIDE REPEAT;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
SYNDROME;
ANODONTIA;
ASIAN CONTINENTAL ANCESTRY GROUP;
CLEFT LIP;
CLEFT PALATE;
CRANIOFACIAL ABNORMALITIES;
DNA MUTATIONAL ANALYSIS;
EXONS;
HUMANS;
INTERFERON REGULATORY FACTORS;
LINKAGE (GENETICS);
MUTATION;
PEDIGREE;
REPETITIVE SEQUENCES, NUCLEIC ACID;
SYNDROME;
MLCS;
MLOWN;
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EID: 33644615691
PISSN: 11073756
EISSN: None
Source Type: Journal
DOI: 10.3892/ijmm.16.5.851 Document Type: Article |
Times cited : (15)
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References (0)
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