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European Journal of Pediatrics|October 1, 1982
Infantile form of sialic acid storage disorder: clinical, ultrastructural, and biochemical studies in two siblingsM Tondeur, J Libert, E Vamos, et al.Journal of Inherited Metabolic Disease|January 1, 1984
Treatment of the cbl B form of methylmalonic acidaemia with adenosylcobalaminM L Batshaw, G H Thomas, S R Cohen, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1975
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblastsH A Taylor, G H Thomas, A Aylsworth, et al.American Journal of Human Genetics|June 1, 1989
Cancer in relatives of leukemic patients with chromosomal rearrangements at rare (heritable) fragile-site locations in their malignant cellsE H Mules, J R Testa, G H Thomas, et al.Molecular Genetics and Metabolism|April 5, 2001
Identification of the alpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferase gene, the human ortholog of the yeast LYS5 geneV Praphanphoj, K A Sacksteder, S J Gould, et al.Cancer Genetics and Cytogenetics|April 12, 2001
A novel variant three-way translocation of inversion 16 in a case of AML-M4eo following low dose methotrexate therapyS Li, R J Couzi, G H Thomas, et al.Human Molecular Genetics|January 1, 1994
Impact of premature stop codons on mRNA levels in infantile Sandhoff diseaseZ X Zhang, N Wakamatsu, E H Mules, et al.Human Genetics|April 1, 1986
Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)]J W Moore, S Hyman, S E Antonarakis, et al.Clinical Chemistry|January 1, 1981
Direct quantitation of glycosaminoglycans in 2 mL of urine from patients with mucopolysaccharidosesR W Burlingame, G H Thomas, R L Stevens, et al.The Journal of Pediatrics|July 1, 1984
Arginine-responsive asymptomatic hyperammonemia in the premature infantM L Batshaw, R C Wachtel, G H Thomas, et al.Pageof 22