Mosaic imprinting defect in a patient with an almost typical expression of the Prader-Willi syndrome.
Wey E; Bartholdi D; Riegel M; Nazlican H; Horsthemke B; Schinzel A; Baumer A; European Journal Of Human Genetics: EJHG, 2005, vol. 13, issue 3, p 273, ISSN 10184813. ISBN 10184813.

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