Search research articles
Contact Us
Filters
Showing results (81-90 of 112) with videos related to
Page
of 12
Sort By:
The Journal of Pediatrics
|
November 5, 1997
Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcome
E Zammarchi, F Ciani, E Pasquini, et al.
Human Genetics
|
June 1, 1987
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes
V Ramesh, R Eddy, G A Bruns, et al.
The New England Journal of Medicine
|
December 31, 1970
Prenatal genetic diagnosis. 3
A Milunsky, J W Littlefield, J N Kanvfer, et al.
Clinical Genetics
|
April 1, 1992
Biochemical investigation of a Brazilian patient with a defect in mitochondrial acetoacetylcoenzyme-A thiolase
M Wajner, M T Sanseverino, R Giugliani, et al.
The New England Journal of Medicine
|
December 24, 1970
Prenatal genetic diagnosis (second of three parts)
A Milunsky, J W Littlefield, J N Kanfer, et al.
The New England Journal of Medicine
|
December 17, 1970
Prenatal genetic diagnosis. I
A Milunsky, J W Littlefield, J N Kanfer, et al.
American Journal of Medical Genetics
|
August 1, 1989
Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death
V E Shih, S M Axel, J C Tewksbury, et al.
Neurology
|
August 28, 2002
Homocysteine, MTHFR 677C-->T polymorphism, and risk of ischemic stroke: results of a meta-analysis
P J Kelly, J Rosand, J P Kistler, et al.
The Journal of Pediatrics
|
March 1, 1978
Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studies
H L Levy, S J Sepe, D S Walton, et al.
Neurology
|
January 29, 2003
Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiency
P J Kelly, K L Furie, J P Kistler, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 112) with videos related to
Sort By:
Page
of 12
The Journal of Pediatrics
|
November 5, 1997
Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcome
E Zammarchi, F Ciani, E Pasquini, et al.
Human Genetics
|
June 1, 1987
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes
V Ramesh, R Eddy, G A Bruns, et al.
The New England Journal of Medicine
|
December 31, 1970
Prenatal genetic diagnosis. 3
A Milunsky, J W Littlefield, J N Kanvfer, et al.
Clinical Genetics
|
April 1, 1992
Biochemical investigation of a Brazilian patient with a defect in mitochondrial acetoacetylcoenzyme-A thiolase
M Wajner, M T Sanseverino, R Giugliani, et al.
The New England Journal of Medicine
|
December 24, 1970
Prenatal genetic diagnosis (second of three parts)
A Milunsky, J W Littlefield, J N Kanfer, et al.
The New England Journal of Medicine
|
December 17, 1970
Prenatal genetic diagnosis. I
A Milunsky, J W Littlefield, J N Kanfer, et al.
American Journal of Medical Genetics
|
August 1, 1989
Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death
V E Shih, S M Axel, J C Tewksbury, et al.
Neurology
|
August 28, 2002
Homocysteine, MTHFR 677C-->T polymorphism, and risk of ischemic stroke: results of a meta-analysis
P J Kelly, J Rosand, J P Kistler, et al.
The Journal of Pediatrics
|
March 1, 1978
Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studies
H L Levy, S J Sepe, D S Walton, et al.
Neurology
|
January 29, 2003
Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiency
P J Kelly, K L Furie, J P Kistler, et al.
Page
of 12