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S Harper

Showing results (441-450 of 1,225) with videos related to

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Advances in Experimental Medicine and Biology|January 1, 1991
Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosisL N al-Jader, M C Goodchild, H C Ryley, et al.
Muscle & Nerve. Supplement|April 12, 2013
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.
Journal of Fluency Disorders|March 26, 2026
A brief treatment program for acquired neurogenic stuttering following cyberknife radiation surgery: An experimental case study report and listener perception studyL De Nil, K Eloise, N Moein, et al.
BMJ (Clinical Research Ed.)|January 21, 1989
Mortality from leukaemia among relatives of patients with cystic fibrosisL N al-Jader, R R West, M C Goodchild, et al.
Journal of Medical Genetics|August 1, 1987
Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales populationL P Lazarou, F Davies, M Sarfarazi, et al.
Biomimetics (Basel, Switzerland)|June 26, 2024
Developing a Biomimetic 3D Neointimal Layer as a Prothrombotic Substrate for a Humanized In Vitro Model of AtherothrombosisJassim Echrish, Madalina-Ioana Pasca, David Cabrera, et al.
American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.
Journal of Medical Genetics|March 2, 1999
Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat lengthP Kehoe, M Krawczak, P S Harper, et al.
Clinical and Experimental Immunology|January 1, 1980
Recurrent meningococcal infections associated with a functional deficiency of the C8 component of human complementN Matthews, J M Stark, P S Harper, et al.
The Biochemical Journal|September 15, 1993
Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblastsD S Anson, V Muller, J Bielicki, et al.
Pageof 123

Showing results (441-450 of 1,225) with videos related to

Sort By:
Pageof 123
Advances in Experimental Medicine and Biology|January 1, 1991
Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosisL N al-Jader, M C Goodchild, H C Ryley, et al.
Muscle & Nerve. Supplement|April 12, 2013
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.
Journal of Fluency Disorders|March 26, 2026
A brief treatment program for acquired neurogenic stuttering following cyberknife radiation surgery: An experimental case study report and listener perception studyL De Nil, K Eloise, N Moein, et al.
BMJ (Clinical Research Ed.)|January 21, 1989
Mortality from leukaemia among relatives of patients with cystic fibrosisL N al-Jader, R R West, M C Goodchild, et al.
Journal of Medical Genetics|August 1, 1987
Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales populationL P Lazarou, F Davies, M Sarfarazi, et al.
Biomimetics (Basel, Switzerland)|June 26, 2024
Developing a Biomimetic 3D Neointimal Layer as a Prothrombotic Substrate for a Humanized In Vitro Model of AtherothrombosisJassim Echrish, Madalina-Ioana Pasca, David Cabrera, et al.
American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.
Journal of Medical Genetics|March 2, 1999
Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat lengthP Kehoe, M Krawczak, P S Harper, et al.
Clinical and Experimental Immunology|January 1, 1980
Recurrent meningococcal infections associated with a functional deficiency of the C8 component of human complementN Matthews, J M Stark, P S Harper, et al.
The Biochemical Journal|September 15, 1993
Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblastsD S Anson, V Muller, J Bielicki, et al.
Pageof 123