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Michael F. Walsh

Johns Hopkins University School of Medicine

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A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1.

2012 American Journal of Medical Genetics Part A
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Interstitial Deletion 5q14.3-q21 Associated With Iris Coloboma, Hearing Loss, Dental Anomaly, Moderate Intellectual Disability, and Attention Deficit and Hyperactivity Disorder

2009 American Journal of Medical Genetics Part A
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