Katherine Christensen
Associate Professor · SSM Health/Saint Louis University School of Medicine
Credentials:
History
Research
Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion
American Journal of Medical Genetics · 1995 · 114 citations
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis
The American Journal of Human Genetics · 2016 · 87 citations
Fabry disease in infancy and early childhood: a systematic literature review
Systematic review or meta-analysis · Genetics in Medicine · 2015 · 78 citations
7 papers
5 papers
3 papers
3 papers
3 papers
- BA
2 papers
- GH
2 papers
2 papers
