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(Stanford University), 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(Cancer Research Institute)
Journal of Medical Genetics
September 1, 2005
10.1136/jmg.2004.028787
Cited by 137

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