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C O Leonard

Showing results (11-20 of 35) with videos related to

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Pediatric Research|August 1, 1971
Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cellsM M Kaback, C O Leonard, T H Parmley
Birth Defects Original Article Series|January 1, 1982
New features of the McKusick-Kaufman syndromeE W Jabs, C O Leonard, J A Phillips
American Journal of Medical Genetics|June 11, 1992
Opitz (BBB/G) syndrome: oral manifestationsJ K Brooks, C O Leonard, P J Coccaro
Annual Review of Public Health|January 1, 1981
Issues in antenatal and neonatal screening and surveillance for hereditary and congenital disordersN A Holtzman, C O Leonard, M R Farfel
Lancet (London, England)|January 25, 1986
Prenatal diagnosis of factor VIII deficiency to help with the management of pregnancy and deliveryB J Baty, D Drayna, C O Leonard, et al.
Journal of Inherited Metabolic Disease|September 10, 2005
Living with phenylketonuria: perspectives of patients and their familiesC Bilginsoy, N Waitzman, C O Leonard, et al.
Clinical Genetics|May 1, 1983
Two different structural abnormalities of chromosome 13 in offspring of chromosomally normal parents with two fragile sitesE H Mules, J Stamberg, E W Jabs, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Adults with Williams syndromeC A Morris, C O Leonard, C Dilts, et al.
The Journal of Pediatrics|December 1, 1990
Late-onset ornithine transcarbamylase deficiency in male patientsJ E Finkelstein, E R Hauser, C O Leonard, et al.
The American Journal of Clinical Nutrition|May 1, 1992
Bone mineral status in children with phenylketonuria--relationship to nutritional intake and phenylalanine controlM P McMurry, G M Chan, C O Leonard, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Pediatric Research|August 1, 1971
Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cellsM M Kaback, C O Leonard, T H Parmley
Birth Defects Original Article Series|January 1, 1982
New features of the McKusick-Kaufman syndromeE W Jabs, C O Leonard, J A Phillips
American Journal of Medical Genetics|June 11, 1992
Opitz (BBB/G) syndrome: oral manifestationsJ K Brooks, C O Leonard, P J Coccaro
Annual Review of Public Health|January 1, 1981
Issues in antenatal and neonatal screening and surveillance for hereditary and congenital disordersN A Holtzman, C O Leonard, M R Farfel
Lancet (London, England)|January 25, 1986
Prenatal diagnosis of factor VIII deficiency to help with the management of pregnancy and deliveryB J Baty, D Drayna, C O Leonard, et al.
Journal of Inherited Metabolic Disease|September 10, 2005
Living with phenylketonuria: perspectives of patients and their familiesC Bilginsoy, N Waitzman, C O Leonard, et al.
Clinical Genetics|May 1, 1983
Two different structural abnormalities of chromosome 13 in offspring of chromosomally normal parents with two fragile sitesE H Mules, J Stamberg, E W Jabs, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Adults with Williams syndromeC A Morris, C O Leonard, C Dilts, et al.
The Journal of Pediatrics|December 1, 1990
Late-onset ornithine transcarbamylase deficiency in male patientsJ E Finkelstein, E R Hauser, C O Leonard, et al.
The American Journal of Clinical Nutrition|May 1, 1992
Bone mineral status in children with phenylketonuria--relationship to nutritional intake and phenylalanine controlM P McMurry, G M Chan, C O Leonard, et al.
Pageof 4