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S Harper

Showing results (691-700 of 1,225) with videos related to

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AJR. American Journal of Roentgenology|December 1, 1987
Hemorrhagic neoplasms: MR mimics of occult vascular malformationsG Sze, G Krol, W L Olsen, et al.
Plastic and Reconstructive Surgery|February 9, 1999
The fetal cleft palate: I. Characterization of a congenital modelJ Weinzweig, K E Panter, M Pantaloni, et al.
Human Genetics|January 1, 1983
Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophyM Sarfarazi, P S Harper, H M Kingston, et al.
American Journal of Human Genetics|September 28, 2000
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helixA J Richards, D M Baguley, J R Yates, et al.
Genomics|November 1, 1992
Genetic heterogeneity in X-linked amelogenesis imperfectaM J Aldred, P J Crawford, E Roberts, et al.
The Journal of Biological Chemistry|March 25, 1989
Carrier-mediated transport of monoiodotyrosine out of thyroid cell lysosomesF Tietze, L D Kohn, A D Kohn, et al.
Human Genetics|December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19qK Johnson, E Nimmo, P Jones, et al.
Journal of Medical Genetics|November 1, 1991
Watson syndrome: is it a subtype of type 1 neurofibromatosis?J E Allanson, M Upadhyaya, G H Watson, et al.
Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.
American Journal of Human Genetics|March 1, 1989
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.
Pageof 123

Showing results (691-700 of 1,225) with videos related to

Sort By:
Pageof 123
AJR. American Journal of Roentgenology|December 1, 1987
Hemorrhagic neoplasms: MR mimics of occult vascular malformationsG Sze, G Krol, W L Olsen, et al.
Plastic and Reconstructive Surgery|February 9, 1999
The fetal cleft palate: I. Characterization of a congenital modelJ Weinzweig, K E Panter, M Pantaloni, et al.
Human Genetics|January 1, 1983
Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophyM Sarfarazi, P S Harper, H M Kingston, et al.
American Journal of Human Genetics|September 28, 2000
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helixA J Richards, D M Baguley, J R Yates, et al.
Genomics|November 1, 1992
Genetic heterogeneity in X-linked amelogenesis imperfectaM J Aldred, P J Crawford, E Roberts, et al.
The Journal of Biological Chemistry|March 25, 1989
Carrier-mediated transport of monoiodotyrosine out of thyroid cell lysosomesF Tietze, L D Kohn, A D Kohn, et al.
Human Genetics|December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19qK Johnson, E Nimmo, P Jones, et al.
Journal of Medical Genetics|November 1, 1991
Watson syndrome: is it a subtype of type 1 neurofibromatosis?J E Allanson, M Upadhyaya, G H Watson, et al.
Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.
American Journal of Human Genetics|March 1, 1989
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.
Pageof 123