Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1
Anne Slavotinek(Cincinnati Children's Hospital Medical Center), Daniel Pinkel(UCSF Helen Diller Family Comprehensive Cancer Center), Ronald W. Davis(Corning (United States)), Kathleen A. Leppig(Group Health Cooperative), S S Lee(University of California, San Francisco), Johng S. Rhim(Group Health Cooperative), A Shrit(Miami Valley Hospital), Katherine M. Jasnosz(Allegheny General Hospital), Donna G. Albertson(New York University)
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