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pro vyhledávání: '"Mei-Chyn Chao"'
Autor:
Hsiang-Yu, Lin, Shuan-Pei, Lin, Chih-Kuang, Chuang, Ming-Ren, Chen, Jui-Lung, Yen, Yann-Jinn, Lee, Chi-Yu, Huang, Li-Ping, Tsai, Dau-Ming, Niu, Mei-Chyn, Chao, Pao-Lin, Kuo
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 96(6)
Several different genetic defects have been found to result in the characteristic phenotypic expression of Prader-Willi syndrome (PWS).We performed a retrospective analysis of 67 cases of molecularly confirmed PWS diagnosed from January 1980 through