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You searched for: Author/Creator Cohen, J.S.

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1. De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. Issue 5 (25th January 2018)

3. Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance. Issue 4 (7th January 2018)

4. Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features. Issue 5 (10th October 2016)