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Histochemistry and Cell Biology|February 7, 1998
Developmental expression of hexokinase 1 and 3 in ratsK A Coerver, S M Gray, J E Barnes, et al.
American Journal of Medical Genetics|July 17, 1995
Rapid molecular cytogenetic analysis of X-chromosomal microdeletions: fluorescence in situ hybridization (FISH) for complex glycerol kinase deficiencyK C Worley, E A Lindsay, W Bailey, et al.
Molecular Genetics and Metabolism|March 6, 1999
Bacterial species identification after DNA amplification with a universal primer pairK M McCabe, Y H Zhang, B L Huang, et al.
American Journal of Medical Genetics|November 15, 1993
Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndromeK A Ellison, E J Roth, E R McCabe, et al.
Biochemical Medicine and Metabolic Biology|December 1, 1994
Hexokinase binding in ischemic and reperfused piglet brainS M Gray, V Adams, Y Yamashita, et al.
Human Genetics|March 1, 1989
Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningD C Jinks, M Minter, D A Tarver, et al.
Genomics|December 1, 1991
Mammalian hexokinase 1: evolutionary conservation and structure to function analysisL D Griffin, B D Gelb, D A Wheeler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiencyS I Goodman, E R McCabe, P V Fennessey, et al.
Biochemical Medicine and Metabolic Biology|April 1, 1989
Synthesis and characterization of a bovine hexokinase 1 cDNA probe by mixed oligonucleotide primed amplification of cDNA using high complexity primer mixturesL D Griffin, G R MacGregor, D M Muzny, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesE Vilain, M Le Merrer, C Lecointre, et al.
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