Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
Slavotinek A; Lee SS; Davis R; Shrit A; Leppig KA; Rhim J; Jasnosz K; Albertson D; Pinkel D; Journal Of Medical Genetics, 2005, vol. 42, issue 9, p 730, ISSN 14686244. ISBN 14686244.

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