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Relationship in the musculo-skeletal syndrome Prader–Willi

✍ Scribed by V. Montangero; R. Capiglioni; E. Roldan


Book ID
116322554
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
98 KB
Volume
45
Category
Article
ISSN
8756-3282

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Several recent studies have suggested the presence of mosaicism for a deletion, detected by fluorescence in situ hybridization (FISH), within chromosome 15q11-q13 in Prader-Willi syndrome (PWS) [Mowery-Rushton et al., 1996;Malzac et al., 1998;Golden et al., 1999]. However, the evidence supporting mo