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N C Nevin

Showing results (191-200 of 223) with videos related to

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Atherosclerosis|February 1, 1996
A novel single base deletion in the LDLR gene (211delG): Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genesA J Ward, M O'Kane, D P Nicholls, et al.
Diabetes|September 1, 1996
A molecular variant of angiotensinogen is associated with diabetic nephropathy in IDDMD G Fogarty, J C Harron, A E Hughes, et al.
Neurology|October 1, 1996
T-cell receptor alpha, beta, gamma, and delta chain gene microsatellites show no association with multiple sclerosisA G Droogan, C W Kirk, S A Hawkins, et al.
Journal of the Neurological Sciences|March 20, 1997
Tumour necrosis factor microsatellites show association with multiple sclerosisC W Kirk, A G Droogan, S A Hawkins, et al.
The British Journal of Dermatology|January 20, 1999
Evidence for a second genetic locus in Carney complexA D Irvine, D K Armstrong, E A Bingham, et al.
Journal of Medical Genetics|November 1, 1996
An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalisA D Irvine, O M Dolan, D R Hadden, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 1, 1997
Von Hippel-Lindau disease: an important differential diagnosis of polycystic kidney diseaseG Browne, J A Jefferson, G D Wright, et al.
Human Molecular Genetics|March 21, 1998
Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysisJ R Yates, I van Bakel, T Sepp, et al.
Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.
Prenatal Diagnosis|September 22, 1998
Early amniocentesis: effect of removing a reduced volume of amniotic fluid on pregnancy outcomeS Tharmaratnam, S Sadek, E K Steele, et al.
Pageof 23

Showing results (191-200 of 223) with videos related to

Sort By:
Pageof 23
Atherosclerosis|February 1, 1996
A novel single base deletion in the LDLR gene (211delG): Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genesA J Ward, M O'Kane, D P Nicholls, et al.
Diabetes|September 1, 1996
A molecular variant of angiotensinogen is associated with diabetic nephropathy in IDDMD G Fogarty, J C Harron, A E Hughes, et al.
Neurology|October 1, 1996
T-cell receptor alpha, beta, gamma, and delta chain gene microsatellites show no association with multiple sclerosisA G Droogan, C W Kirk, S A Hawkins, et al.
Journal of the Neurological Sciences|March 20, 1997
Tumour necrosis factor microsatellites show association with multiple sclerosisC W Kirk, A G Droogan, S A Hawkins, et al.
The British Journal of Dermatology|January 20, 1999
Evidence for a second genetic locus in Carney complexA D Irvine, D K Armstrong, E A Bingham, et al.
Journal of Medical Genetics|November 1, 1996
An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalisA D Irvine, O M Dolan, D R Hadden, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 1, 1997
Von Hippel-Lindau disease: an important differential diagnosis of polycystic kidney diseaseG Browne, J A Jefferson, G D Wright, et al.
Human Molecular Genetics|March 21, 1998
Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysisJ R Yates, I van Bakel, T Sepp, et al.
Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.
Prenatal Diagnosis|September 22, 1998
Early amniocentesis: effect of removing a reduced volume of amniotic fluid on pregnancy outcomeS Tharmaratnam, S Sadek, E K Steele, et al.
Pageof 23