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Volumn 62 Suppl 3, Issue , 2004, Pages 60-65
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Molecular basis of Sotos syndrome.
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Author keywords
[No Author keywords available]
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Indexed keywords
NSD1 PROTEIN, HUMAN;
NUCLEAR PROTEIN;
SIGNAL PEPTIDE;
BRAIN;
CONGENITAL MALFORMATION;
GENE DELETION;
GENETIC PREDISPOSITION;
GENETICS;
GENOTYPE;
GIGANTISM;
HUMAN;
NEOPLASM;
PATHOLOGY;
PHENOTYPE;
REVIEW;
SYNDROME;
BRAIN;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
GIGANTISM;
HUMANS;
INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS;
NEOPLASMS;
NUCLEAR PROTEINS;
PHENOTYPE;
SEQUENCE DELETION;
SYNDROME;
MLCS;
MLOWN;
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EID: 21644437055
PISSN: 03010163
EISSN: None
Source Type: Journal
DOI: 10.1159/000080501 Document Type: Review |
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Times cited : (22)
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References (19)
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