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W K Seltzer

Showing results (11-20 of 34) with videos related to

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Journal of Child Neurology|February 24, 2001
Fatal infantile X-linked neuropathyE Sekul, J E Carroll, F Yaghmai, et al.
American Journal of Human Genetics|October 1, 1992
Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophyL S Schwartz, J Tarleton, B Popovich, et al.
Muscle & Nerve|April 1, 1989
Muscle glycerol kinase in Duchenne dystrophy and glycerol kinase deficiencyW K Seltzer, C Angelini, G Dhariwal, et al.
Biochemical Medicine|April 1, 1985
Adrenal dysfunction in glycerol kinase deficiencyW K Seltzer, H Firminger, J Klein, et al.
Neurology|January 1, 1994
Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspringT Ashizawa, P W Dunne, P A Ward, et al.
Journal of the Neurological Sciences|July 3, 2007
Rare myelin protein zero sequence variant in late onset CMT1BNizar Souayah, W K Seltzer, Thomas H Brannagan, et al.
Hemoglobin|January 1, 1992
Molecular genetic studies in black families with sickle cell anemia and unusually high levels of fetal hemoglobinW K Seltzer, T C Abshire, P A Lane, et al.
The Journal of Pediatrics|April 1, 1993
Relationship of genotype to early pulmonary function in infants with cystic fibrosis identified through neonatal screeningR T Mohon, J S Wagener, S H Abman, et al.
Biochemical Medicine and Metabolic Biology|February 1, 1988
Blood phenylalanine estimation for the patient with phenylketonuria using a portable deviceK Peterson, R Slover, S Gass, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Human glycerol kinase deficiency: enzyme kinetics and fibroblast hybridizationE R McCabe, D Sadava, W W Bullen, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Journal of Child Neurology|February 24, 2001
Fatal infantile X-linked neuropathyE Sekul, J E Carroll, F Yaghmai, et al.
American Journal of Human Genetics|October 1, 1992
Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophyL S Schwartz, J Tarleton, B Popovich, et al.
Muscle & Nerve|April 1, 1989
Muscle glycerol kinase in Duchenne dystrophy and glycerol kinase deficiencyW K Seltzer, C Angelini, G Dhariwal, et al.
Biochemical Medicine|April 1, 1985
Adrenal dysfunction in glycerol kinase deficiencyW K Seltzer, H Firminger, J Klein, et al.
Neurology|January 1, 1994
Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspringT Ashizawa, P W Dunne, P A Ward, et al.
Journal of the Neurological Sciences|July 3, 2007
Rare myelin protein zero sequence variant in late onset CMT1BNizar Souayah, W K Seltzer, Thomas H Brannagan, et al.
Hemoglobin|January 1, 1992
Molecular genetic studies in black families with sickle cell anemia and unusually high levels of fetal hemoglobinW K Seltzer, T C Abshire, P A Lane, et al.
The Journal of Pediatrics|April 1, 1993
Relationship of genotype to early pulmonary function in infants with cystic fibrosis identified through neonatal screeningR T Mohon, J S Wagener, S H Abman, et al.
Biochemical Medicine and Metabolic Biology|February 1, 1988
Blood phenylalanine estimation for the patient with phenylketonuria using a portable deviceK Peterson, R Slover, S Gass, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Human glycerol kinase deficiency: enzyme kinetics and fibroblast hybridizationE R McCabe, D Sadava, W W Bullen, et al.
Pageof 4