Prader-Willi syndrome (PWS) is a genomic imprinting disorder, which is due to the loss of a functional paternal copy of 15q11-q13. Four different genetic mechanisms can lead to PWS: a paternal deletion of the 15q11-q13 region, maternal uniparental disomy (UPD), a defect in the imprinting center, or
β¦ LIBER β¦
Investigation of thermoregulatory characteristics in patients with Prader-Willi syndrome
β Scribed by Williams, Marc S. ;Rooney, Brenda L. ;Williams, Janet ;Josephson, Kevin ;Pauli, Richard
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 592 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0148-7299
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