Mosaicism in Prader-Willi syndrome
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Nicholls, Robert D.
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Article
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2000
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John Wiley and Sons
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English
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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