Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Kim SJ; Miller JL; Kuipers PJ; German JR; Beaudet AL; Sahoo T; Driscoll DJ; European Journal Of Human Genetics: EJHG, 2012, vol. 20, issue 3, p 283, ISSN 14765438. ISBN 14765438.

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