The Angelman (AS) and Prader±Willi syndromes (PWS) are clinically distinct neurobehavioural syndromes resulting from loss of maternal (AS) or paternal contributions (PWS) of imprinted genes within the chromosomal 15q11-q13 region. The molecular diagnosis of both syndromes can be made by a variety of
✦ LIBER ✦
Prenatal diagnosis and the Prader-Willi syndrome
✍ Scribed by Arabella Smith
- Publisher
- Springer
- Year
- 1986
- Tongue
- English
- Weight
- 57 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0340-6717
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