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Showing results (61-70 of 65) with videos related to

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Neurochemistry International|March 20, 2002
Inhibition of the mitochondrial respiratory chain complex activities in rat cerebral cortex by methylmalonic acidA M Brusque, R Borba Rosa, P F Schuck, et al.
Revista De Neurologia|April 1, 2003
[Severe fulminant form of neonatal citrullinemia. Report of a case]P Lalaguna-Mallada, R García-Romero, B Alonso-del Val, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated familiesW J Kleijer, V H Garritsen, M Linnebank, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
Potential relationship between genotype and clinical outcome in propionic acidaemia patientsC Pérez-Cerdá, B Merinero, P Rodríguez-Pombo, et al.
Heredity|July 30, 2009
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutationsJ M Flanagan, G McMahon, S H Brendan Chia, et al.
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Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Neurochemistry International|March 20, 2002
Inhibition of the mitochondrial respiratory chain complex activities in rat cerebral cortex by methylmalonic acidA M Brusque, R Borba Rosa, P F Schuck, et al.
Revista De Neurologia|April 1, 2003
[Severe fulminant form of neonatal citrullinemia. Report of a case]P Lalaguna-Mallada, R García-Romero, B Alonso-del Val, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated familiesW J Kleijer, V H Garritsen, M Linnebank, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
Potential relationship between genotype and clinical outcome in propionic acidaemia patientsC Pérez-Cerdá, B Merinero, P Rodríguez-Pombo, et al.
Heredity|July 30, 2009
The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutationsJ M Flanagan, G McMahon, S H Brendan Chia, et al.
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