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M J Mahoney

Showing results (81-90 of 187) with videos related to

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Birth Defects Original Article Series|January 1, 1974
A renal lesion in asphyxiating thoracic dysplasiaP J Edelson, T J Spackman, R E Belliveau, et al.
The Journal of Clinical Investigation|November 1, 1975
Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblastsH L Bonkowsky, J R Bloomer, P S Ebert, et al.
Experimental Cell Research|May 1, 1975
Electron microscopy of human skin fibroblasts in situ during growth in cultureA W Lucky, M J Mahoney, R J Barrnett, et al.
Journal of Medical Genetics|May 1, 1989
Deletion (12)(q15q21.2)M S Watson, L McAllister-Barton, M J Mahoney, et al.
American Journal of Obstetrics and Gynecology|April 15, 1982
Stage II ultrasound examination for the diagnosis of fetal abnormalities with an elevated amniotic fluid alpha-fetoprotein concentrationJ C Hobbins, I Venus, M Tortora, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1975
Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesisM J Mahoney, A C Hart, V D Steen, et al.
Lancet (London, England)|July 31, 1976
Inheritance in protoporphyria. Comparison of haem synthetase activity in skin fibroblasts with clinical featuresJ R Bloomer, H L Bonkowsky, P S Ebert, et al.
Lancet (London, England)|December 9, 1978
False-negative A.F.P. screen for congenital nephrosis Finnish typeR A Spritz, S J Soiffer, N J Siegel, et al.
Pediatrics|March 1, 1978
A case of short rib polydactylyP Bidot-López, R C Ablow, J A Ogden, et al.
Acta Paediatrica Scandinavica|January 1, 1975
Prenatal diagnosis of methylmalonic aciduriaM J Mahoney, L E Rosenberg, B Lindblad, et al.
Pageof 19

Showing results (81-90 of 187) with videos related to

Sort By:
Pageof 19
Birth Defects Original Article Series|January 1, 1974
A renal lesion in asphyxiating thoracic dysplasiaP J Edelson, T J Spackman, R E Belliveau, et al.
The Journal of Clinical Investigation|November 1, 1975
Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblastsH L Bonkowsky, J R Bloomer, P S Ebert, et al.
Experimental Cell Research|May 1, 1975
Electron microscopy of human skin fibroblasts in situ during growth in cultureA W Lucky, M J Mahoney, R J Barrnett, et al.
Journal of Medical Genetics|May 1, 1989
Deletion (12)(q15q21.2)M S Watson, L McAllister-Barton, M J Mahoney, et al.
American Journal of Obstetrics and Gynecology|April 15, 1982
Stage II ultrasound examination for the diagnosis of fetal abnormalities with an elevated amniotic fluid alpha-fetoprotein concentrationJ C Hobbins, I Venus, M Tortora, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1975
Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesisM J Mahoney, A C Hart, V D Steen, et al.
Lancet (London, England)|July 31, 1976
Inheritance in protoporphyria. Comparison of haem synthetase activity in skin fibroblasts with clinical featuresJ R Bloomer, H L Bonkowsky, P S Ebert, et al.
Lancet (London, England)|December 9, 1978
False-negative A.F.P. screen for congenital nephrosis Finnish typeR A Spritz, S J Soiffer, N J Siegel, et al.
Pediatrics|March 1, 1978
A case of short rib polydactylyP Bidot-López, R C Ablow, J A Ogden, et al.
Acta Paediatrica Scandinavica|January 1, 1975
Prenatal diagnosis of methylmalonic aciduriaM J Mahoney, L E Rosenberg, B Lindblad, et al.
Pageof 19