Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect. (Q40884892)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect. |
scientific article |
Statements
Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect (English)
A Schulze
C Hansen
P Baekgaard
S Blichfeldt
M B Petersen
N Tommerup
K Brøndum-Nielsen
1 August 1997