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Identification of a Mutation in VPS13B , the Cohen Syndrome Gene, in a... | Download Scientific Diagram
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Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome | Journal of Medical Genetics
Ketuvot 23b ~ The Cohen Gene — Talmudology
Disease relevance of rare VPS13B missense variants for neurodevelopmental Cohen syndrome | Scientific Reports
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About The Founder :: Gene D. Cohen, MD, Ph.D (1944 – 2009)
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Ketuvot 23b ~ The Cohen Gene — Talmudology
Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport - ScienceDirect