Fryns syndrome phenolype caused by chromosome microdeletions at 15q26.2 and 8pZ3.1.
Slavotinek, A.; Lee, S. S.; Davis, R.; Shrit, A.; Leppig, K. A.; Rhim, J.; Jasnosz, K.; Albertson, D.; Pinkel, D.; Journal of Medical Genetics, 2005, vol. 42, issue 9, p 730, ISSN 00222593. ISBN 14686244.

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