Publications by authors named "Mohammed S Rashed"

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Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.
Moeenaldeen Al-Sayed, Faiqa Imtiaz, Osama A Alsmadi, Mohammed S Rashed, Brian F Meyer

BMC Med Genet· December 2006

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Goldenhar syndrome and hereditary tyrosinemia type 1.
Moeen A Al-Sayed, Ali M Al-Asmari, Mohammed S Rashed

Neurosciences (Riyadh)· January 2003

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Goldenhar syndrome and hereditary tyrosinemia type 1.
Moeen A Al-Sayed, Ali M Asmari, Mohammed S Rashed

Saudi Med J· December 2002

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