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Publications by S G Kahler

Double Mutant Fibrillin-1 (FBN1) Allele in a Patient With Neonatal Marfan Syndrome.

Journal of Medical Genetics

English

Intravenous L-Carnitine and Acetyl-L-Carnitine in Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency and Isovaleric Acidemia

Pediatric Research

English