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Prader–Willi syndrome in Taiwan

✍ Scribed by HSIANG-YU LIN; SHUAN-PEI LIN; JUI-LUNG YEN; YANN-JINN LEE; CHI-YU HUANG; HAN-YANG HUNG; CHYONG-HSIN HSU; HSIN-AN KAO; JUI-HSING CHANG; NAN-CHANG CHIU; CHE-SHENG HO; MEI-CHYN CHAO; DAU-MING NIU; LI-PING TSAI; PAO-LIN KUO

Book ID
108971287
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
209 KB
Volume
49
Category
Article
ISSN
1328-8067

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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