Wendy Smith
Physician · MaineHealth - Maine Medical Center
Credentials: · · · ·
History
Research
Phenylalanine hydroxylase deficiency: diagnosis and management guideline
Genetics in Medicine · 2014 · 510 citations
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification
Nature Genetics · 2003 · 491 citations
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Nature Genetics · 2010 · 478 citations
15 papers
14 papers
14 papers
13 papers
13 papers
- GD
12 papers
12 papers
- CH
11 papers
