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Volumn 68, Issue 1, 2001, Pages 81-91
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Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III
a b d a a a c e a f g i j k l m n o p q more.. |
Author keywords
[No Author keywords available]
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Indexed keywords
DNA BINDING PROTEIN;
TRANSCRIPTION FACTOR GATA 1;
ZINC FINGER PROTEIN;
ARTICLE;
BRACHYDACTYLY;
CHROMOSOME 8;
CLINICAL FEATURE;
CONTROLLED STUDY;
CORRELATION FUNCTION;
CRANIOFACIAL MALFORMATION;
DISEASE CLASSIFICATION;
EXOSTOSIS;
GENE DELETION;
GENE MUTATION;
GENOTYPE;
HUMAN;
HUMAN CELL;
MISSENSE MUTATION;
NUCLEOTIDE SEQUENCE;
PHENOTYPE;
PRIORITY JOURNAL;
PROTEIN DNA BINDING;
SKELETON MALFORMATION;
TRICHORHINOPHALANGEAL SYNDROME;
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EID: 0035159093
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: 10.1086/316926 Document Type: Article |
Times cited : (188)
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References (31)
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