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Journal of Inherited Metabolic Disease|January 5, 2002
Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiencyG T Berry, T Fukao, G A Mitchell, et al.
Plos One|November 17, 2012
ERMO3/MVP1/GOLD36 is involved in a cell type-specific mechanism for maintaining ER morphology in Arabidopsis thalianaRyohei Thomas Nakano, Ryo Matsushima, Atsushi J Nagano, et al.
Prenatal Diagnosis|May 1, 1996
Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.
Biochemical and Biophysical Research Communications|January 28, 1994
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.
Journal of Epidemiology|April 5, 2003
The relationship of thyroid cancer with radiation exposure from nuclear weapon testing in the Marshall IslandsTatsuya Takahashi, Minouk J Schoemaker, Klaus R Trott, et al.
International Journal of Cancer|January 6, 2007
Coffee consumption and the risk of colorectal cancer: a prospective cohort study in JapanToru Naganuma, Shinichi Kuriyama, Munira Akhter, et al.
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