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R G Gray

Showing results (51-60 of 101) with videos related to

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Developmental Medicine and Child Neurology|August 1, 1985
Glutaric aciduria type I misdiagnosed as Leigh's encephalopathy and cerebral palsyP Stutchfield, M A Edwards, R G Gray, et al.
British Journal of Haematology|October 1, 1988
Terminal deoxynucleotidyl transferase and HLA-DR expression appear unrelated to prognosis of acute myeloid leukaemiaD M Swirsky, M F Greaves, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twinsR G Gray, A D Patrick, F E Preston, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|September 12, 2001
Intraoral molluscum contagiosum: a report of a case and a review of the literatureM L Fornatora, R F Reich, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Acute neonatal citrullinaemiaM J Bennett, P R Dear, J M McGinlay, et al.
Pediatric Research|November 1, 1976
Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratiosR G Gray, J A Black, V H Lyons, et al.
Journal of Adolescent Health Care : Official Publication of the Society for Adolescent Medicine|March 1, 1983
The relationship between physical activity and serum lipids and lipoproteins in black children and adolescentsR H Durant, C W Linder, J W Harkess, et al.
Annals of Clinical Biochemistry|May 1, 1977
Enzyme studies on a new case of ornithine carbamoyl transferase deficiency: remaining problems and a method of diagnosis based on plasma enzyme ratiosR J Pollitt, J A Black, R G Gray, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1987
A myelodysplastic syndrome with marrow eosinophilia terminating in acute nonlymphocytic leukemia, associated with an abnormal chromosome 16S L Abbondanzo, R G Gray, J Whang-Peng, et al.
Developmental Medicine and Child Neurology|September 24, 1998
A case of Ohtahara syndrome with cytochrome oxidase deficiencyA N Williams, R G Gray, K Poulton, et al.
Pageof 11

Showing results (51-60 of 101) with videos related to

Sort By:
Pageof 11
Developmental Medicine and Child Neurology|August 1, 1985
Glutaric aciduria type I misdiagnosed as Leigh's encephalopathy and cerebral palsyP Stutchfield, M A Edwards, R G Gray, et al.
British Journal of Haematology|October 1, 1988
Terminal deoxynucleotidyl transferase and HLA-DR expression appear unrelated to prognosis of acute myeloid leukaemiaD M Swirsky, M F Greaves, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twinsR G Gray, A D Patrick, F E Preston, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|September 12, 2001
Intraoral molluscum contagiosum: a report of a case and a review of the literatureM L Fornatora, R F Reich, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Acute neonatal citrullinaemiaM J Bennett, P R Dear, J M McGinlay, et al.
Pediatric Research|November 1, 1976
Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratiosR G Gray, J A Black, V H Lyons, et al.
Journal of Adolescent Health Care : Official Publication of the Society for Adolescent Medicine|March 1, 1983
The relationship between physical activity and serum lipids and lipoproteins in black children and adolescentsR H Durant, C W Linder, J W Harkess, et al.
Annals of Clinical Biochemistry|May 1, 1977
Enzyme studies on a new case of ornithine carbamoyl transferase deficiency: remaining problems and a method of diagnosis based on plasma enzyme ratiosR J Pollitt, J A Black, R G Gray, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1987
A myelodysplastic syndrome with marrow eosinophilia terminating in acute nonlymphocytic leukemia, associated with an abnormal chromosome 16S L Abbondanzo, R G Gray, J Whang-Peng, et al.
Developmental Medicine and Child Neurology|September 24, 1998
A case of Ohtahara syndrome with cytochrome oxidase deficiencyA N Williams, R G Gray, K Poulton, et al.
Pageof 11