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PHENOTYPE/GENOTYPE CORRELATIONS FOR CONTIGUOUS GENE DELETION SYNDROMES

$35,952M01FY2000RRNIH

Baylor College Of Medicine, Houston TX

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Abstract

In this protocol, phenotypic characterization and systematic evaluation of specific organ system development are correlated with ongoing molecular analysis of contiguous gene syndromes in patients having Williams Syndrome, Smith-Magenis Syndrome, Prader-Willi Syndrome and DiGeorge/Velo-Cardio-Facial Syndrome.

View original record on NIH RePORTER →