Stacie D. Adams
Medical Genetics | Pediatrics
35 Michigan St NE Ste 3003
Grand Rapids, MI 49503
Grand Rapids, MI 49503
Last Updated: 09/26/2026
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Found 7 publications
Case of an unreported genetic variant of salt losing 3-β-hydroxysteroid dehydrogenase deficiency.
Journal: Oxford medical case reports
Published: September 08, 2020
Rapid whole-genome sequencing identifies a homozygous novel variant, His540Arg, in HSD17B4 resulting in D-bifunctional protein deficiency disorder diagnosis.
Journal: Cold Spring Harbor molecular case studies
Published: June 18, 2020
Acute Liver Failure Secondary to Neuroblastoma Amplified Sequence Deficiency.
Journal: The Journal of pediatrics
Published: November 29, 2016
Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
Journal: American journal of medical genetics. Part A
Published: November 16, 2014
Direct-to-consumer genomic testing offers little clinical utility but appears to cause minimal harm.
Direct-to-consumer genomic testing offers little clinical utility but appears to cause minimal harm.
Journal: North Carolina medical journal
Published: December 10, 2013
EPC mobilization after erythropoietin treatment in acute ST-elevation myocardial infarction: the REVEAL EPC substudy.
Journal: Journal of thrombosis and thrombolysis
Published: May 24, 2013
A 19-year-old man with sickle cell disease presenting with spinal infarction: a case report.
Journal: Journal of medical case reports
Published: January 30, 2013
Showing 1-7 of 7
Last Updated: 09/26/2026