ISCA-37392-Loss

7q11.23 recurrent (Williams-Beuren syndrome) region (includes ELN) Loss
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
194050, Williams syndrome