Concurrent diagnoses of Prader–Willi syndrome and GM2 gangliosidosis caused by uniparental disomy of chromosome 15

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|167|8|1944-1948

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.167, Iss.8, 2015-08, pp. : 1944-1948

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