PM
Paul Mark
Physician · Corewell Health West
Credentials: · · · ·
History
Research
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Nature Genetics · 2010 · 478 citations
NAD Deficiency, Congenital Malformations, and Niacin Supplementation
New England Journal of Medicine · 2017 · 199 citations
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
Nature Genetics · 2021 · 89 citations
4 papers
3 papers
3 papers
- FA
3 papers
3 papers
2 papers
2 papers
2 papers
