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.
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