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P S Gerald

Showing results (31-40 of 66) with videos related to

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Pediatrics|January 1, 1970
Clinical and biochemical observations of patients with atypical phenylketonuriaE S Kang, S Kaufman, P S Gerald
American Journal of Human Genetics|March 1, 1971
A second family with the nail-patella allele and the adenylate kinase allele in couplingR S Sobel, A Tiger, P S Gerald
Journal of Autism and Developmental Disorders|September 1, 1982
Infantile autism associated with the fragile-X syndromeD L Meryash, L S Szymanski, P S Gerald
The Journal of Pediatrics|April 1, 1973
Ornithine transcarbamylase deficiency in the newborn infantE S Kang, P J Snodgrass, P S Gerald
Cytogenetics and Cell Genetics|January 1, 1976
Human mitochondrial NADP-dependent isocitrate dehydrogenase in man-mouse somatic cell hybridsG A Bruns, R E Eisenman, P S Gerald
Pediatrics|December 1, 1970
Results of treatment and termination of the diet in phenylketonuria (PKU)E S Kang, N D Sollee, P S Gerald
Pediatric Research|December 1, 1972
Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduriaE S Kang, P J Snodgrass, P S Gerald
Chromosoma|August 17, 1976
BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomesS A Latt, H F Willard, P S Gerald
Neurology|May 1, 1970
Homocystinuria. Response to pyridoxineE S Kang, R K Byers, P S Gerald
Pediatrics|November 1, 1984
Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infantR Carmi, D L Meryash, J Wood, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
Pediatrics|January 1, 1970
Clinical and biochemical observations of patients with atypical phenylketonuriaE S Kang, S Kaufman, P S Gerald
American Journal of Human Genetics|March 1, 1971
A second family with the nail-patella allele and the adenylate kinase allele in couplingR S Sobel, A Tiger, P S Gerald
Journal of Autism and Developmental Disorders|September 1, 1982
Infantile autism associated with the fragile-X syndromeD L Meryash, L S Szymanski, P S Gerald
The Journal of Pediatrics|April 1, 1973
Ornithine transcarbamylase deficiency in the newborn infantE S Kang, P J Snodgrass, P S Gerald
Cytogenetics and Cell Genetics|January 1, 1976
Human mitochondrial NADP-dependent isocitrate dehydrogenase in man-mouse somatic cell hybridsG A Bruns, R E Eisenman, P S Gerald
Pediatrics|December 1, 1970
Results of treatment and termination of the diet in phenylketonuria (PKU)E S Kang, N D Sollee, P S Gerald
Pediatric Research|December 1, 1972
Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduriaE S Kang, P J Snodgrass, P S Gerald
Chromosoma|August 17, 1976
BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomesS A Latt, H F Willard, P S Gerald
Neurology|May 1, 1970
Homocystinuria. Response to pyridoxineE S Kang, R K Byers, P S Gerald
Pediatrics|November 1, 1984
Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infantR Carmi, D L Meryash, J Wood, et al.
Pageof 7