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S Jeffery

Showing results (141-150 of 181) with videos related to

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American Journal of Human Genetics|June 5, 2001
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtypeH Patel, P E Hart, T T Warner, et al.
British Heart Journal|December 1, 1992
Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reactionP J Keeling, S Jeffery, A L Caforio, et al.
Journal of Medical Genetics|February 4, 2005
Milroy disease and the VEGFR-3 mutation phenotypeG Brice, A H Child, A Evans, et al.
Journal of Medical Genetics|September 10, 2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedemaA L Evans, R Bell, G Brice, et al.
Clinical Genetics|January 14, 2012
CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalisF C Connell, K Kalidas, P Ostergaard, et al.
Journal of Anatomy|August 7, 2025
Factors impacting the complexity of the leporid intracranial jointAmber P Wood-Bailey, Heather E White, Samuel R R Cross, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|July 9, 2002
Are cysteinyl leukotrienes involved in allergic responses in human skin?M K Church, T J Griffiths, S Jeffery, et al.
Lancet (London, England)|July 21, 2000
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)G McKoy, N Protonotarios, A Crosby, et al.
Journal of Hypertension|August 1, 1994
Angiotensin converting enzyme insertion/deletion polymorphism: association with ethnic originJ Barley, A Blackwood, N D Carter, et al.
Clinical Science (London, England : 1979)|September 9, 1998
Methylenetetrahydrofolate reductase polymorphism (C-677T) and coronary artery diseaseN M Malik, P Syrris, R Schwartzman, et al.
Pageof 19

Showing results (141-150 of 181) with videos related to

Sort By:
Pageof 19
American Journal of Human Genetics|June 5, 2001
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtypeH Patel, P E Hart, T T Warner, et al.
British Heart Journal|December 1, 1992
Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reactionP J Keeling, S Jeffery, A L Caforio, et al.
Journal of Medical Genetics|February 4, 2005
Milroy disease and the VEGFR-3 mutation phenotypeG Brice, A H Child, A Evans, et al.
Journal of Medical Genetics|September 10, 2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedemaA L Evans, R Bell, G Brice, et al.
Clinical Genetics|January 14, 2012
CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalisF C Connell, K Kalidas, P Ostergaard, et al.
Journal of Anatomy|August 7, 2025
Factors impacting the complexity of the leporid intracranial jointAmber P Wood-Bailey, Heather E White, Samuel R R Cross, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|July 9, 2002
Are cysteinyl leukotrienes involved in allergic responses in human skin?M K Church, T J Griffiths, S Jeffery, et al.
Lancet (London, England)|July 21, 2000
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)G McKoy, N Protonotarios, A Crosby, et al.
Journal of Hypertension|August 1, 1994
Angiotensin converting enzyme insertion/deletion polymorphism: association with ethnic originJ Barley, A Blackwood, N D Carter, et al.
Clinical Science (London, England : 1979)|September 9, 1998
Methylenetetrahydrofolate reductase polymorphism (C-677T) and coronary artery diseaseN M Malik, P Syrris, R Schwartzman, et al.
Pageof 19