Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder
Mol Genet Metab
.
1999 May;67(1):1-10.
doi: 10.1006/mgme.1999.2844.
Author
L R Osborne
1
Affiliation
1
Department of Genetics & Genomic Biology, The Hospital for Sick Children, 555 University Avenue, Toronto, M5G 1X8, Canada.
PMID:
10329018
DOI:
10.1006/mgme.1999.2844
No abstract available
Publication types
Review
MeSH terms
Chromosome Mapping
Chromosomes, Human, Pair 7
Elastin / genetics
Gene Deletion*
Genotype
Humans
Phenotype
Williams Syndrome / genetics*
Substances
Elastin