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Showing articles 0 to 6 of 6

Filter Applied: molecular genetics (Click to remove)

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995



Showing articles 0 to 6 of 6