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S Jeffery

Showing results (91-100 of 181) with videos related to

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FEBS Letters|March 26, 1990
Chronic stimulation-induced effects point to a coordinated expression of carbonic anhydrase III and slow myosin heavy chain in skeletal muscleS Jeffery, C D Kelly, N Carter, et al.
Journal of Human Hypertension|June 1, 1996
Factor V Leiden polymorphism (FV Q506) in patients with ischaemic heart disease, and in different populations groupsS Jeffery, E Leatham, Y Zhang, et al.
Clinical Genetics|April 5, 2013
A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation familyG Brice, P Ostergaard, S Jeffery, et al.
Clinical Genetics|June 1, 1995
Genetic analysis of 20 families with autosomal dominant adult polycystic kidney disease from South West Thames RegionS Jeffery, A K Saggar-Malik, S Morgan, et al.
The Journal of Endocrinology|July 1, 1986
Effects of hypophysectomy and growth hormone infusion on rat hepatic carbonic anhydrasesS Jeffery, C A Wilson, A Mode, et al.
Archives of Disease in Childhood|September 23, 2006
The natural history of Noonan syndrome: a long-term follow-up studyA C Shaw, K Kalidas, A H Crosby, et al.
Clinical Genetics|February 21, 2007
A family with lymphoedema-distichiasis where identical twins have a discordant phenotypeS Kumar, C Carver, S McCall, et al.
American Journal of Hypertension|March 4, 2000
Angiotensin-converting enzyme gene I/D polymorphism and carotid artery disease in renovascular hypertensionA Losito, A Selvi, S Jeffery, et al.
Journal of Medical Genetics|June 1, 1995
A family with autosomal dominant polycystic kidney disease linked to 4q21-23S Jeffery, S Morgan, V J Warmington, et al.
Journal of Medical Genetics|June 1, 1990
Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome)N D Carter, J E Morgan, A P Monaco, et al.
Pageof 19

Showing results (91-100 of 181) with videos related to

Sort By:
Pageof 19
FEBS Letters|March 26, 1990
Chronic stimulation-induced effects point to a coordinated expression of carbonic anhydrase III and slow myosin heavy chain in skeletal muscleS Jeffery, C D Kelly, N Carter, et al.
Journal of Human Hypertension|June 1, 1996
Factor V Leiden polymorphism (FV Q506) in patients with ischaemic heart disease, and in different populations groupsS Jeffery, E Leatham, Y Zhang, et al.
Clinical Genetics|April 5, 2013
A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation familyG Brice, P Ostergaard, S Jeffery, et al.
Clinical Genetics|June 1, 1995
Genetic analysis of 20 families with autosomal dominant adult polycystic kidney disease from South West Thames RegionS Jeffery, A K Saggar-Malik, S Morgan, et al.
The Journal of Endocrinology|July 1, 1986
Effects of hypophysectomy and growth hormone infusion on rat hepatic carbonic anhydrasesS Jeffery, C A Wilson, A Mode, et al.
Archives of Disease in Childhood|September 23, 2006
The natural history of Noonan syndrome: a long-term follow-up studyA C Shaw, K Kalidas, A H Crosby, et al.
Clinical Genetics|February 21, 2007
A family with lymphoedema-distichiasis where identical twins have a discordant phenotypeS Kumar, C Carver, S McCall, et al.
American Journal of Hypertension|March 4, 2000
Angiotensin-converting enzyme gene I/D polymorphism and carotid artery disease in renovascular hypertensionA Losito, A Selvi, S Jeffery, et al.
Journal of Medical Genetics|June 1, 1995
A family with autosomal dominant polycystic kidney disease linked to 4q21-23S Jeffery, S Morgan, V J Warmington, et al.
Journal of Medical Genetics|June 1, 1990
Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome)N D Carter, J E Morgan, A P Monaco, et al.
Pageof 19