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N C Nevin

Showing results (171-180 of 223) with videos related to

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Eye (London, England)|January 1, 1990
DNA analysis and recombination in X-linked retinitis pigmentosaR M Redmond, C A Graham, I W Craig, et al.
Lancet (London, England)|February 2, 1991
Presymptomatic screening for MEN-2AP J Morrison, N C Nevin, A E Hughes, et al.
Human Genetics|November 1, 1989
Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern IrelandA J Hill, C A Graham, E D Kelly, et al.
Lancet (London, England)|April 2, 1994
ACE gene typingD G Fogarty, A P Maxwell, C C Doherty, et al.
American Journal of Medical Genetics|March 29, 1996
Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextropositionA D Irvine, F J Stewart, E A Bingham, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1993
Autosomal dominant polycystic kidney disease with minimal clinical expression unlinked to the PKD1 locusG D Wright, A E Hughes, K A Larkin, et al.
Human Genetics|January 1, 1981
Detection of cystic fibrosis homozygotes and heterozygotes by serum isoelectrofocusingG B Nevin, N C Nevin, A O Redmond, et al.
British Journal of Obstetrics and Gynaecology|March 21, 1998
Transplacental early amniocentesis and pregnancy outcomeS Tharmaratnam, S Sadek, E K Steele, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Contiguous gene deletion syndrome involving glycerol kinase and Duchenne muscular dystrophy lociM Asghar, N C Nevin, E D Beattie, et al.
Human Mutation|January 1, 1995
Three novel mutations in the EGF precursor homology domain of the low-density lipoprotein receptor gene in Northern Irish patients with familial hypercholesterolemiaA J Ward, M O'Kane, I Young, et al.
Pageof 23

Showing results (171-180 of 223) with videos related to

Sort By:
Pageof 23
Eye (London, England)|January 1, 1990
DNA analysis and recombination in X-linked retinitis pigmentosaR M Redmond, C A Graham, I W Craig, et al.
Lancet (London, England)|February 2, 1991
Presymptomatic screening for MEN-2AP J Morrison, N C Nevin, A E Hughes, et al.
Human Genetics|November 1, 1989
Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern IrelandA J Hill, C A Graham, E D Kelly, et al.
Lancet (London, England)|April 2, 1994
ACE gene typingD G Fogarty, A P Maxwell, C C Doherty, et al.
American Journal of Medical Genetics|March 29, 1996
Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextropositionA D Irvine, F J Stewart, E A Bingham, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1993
Autosomal dominant polycystic kidney disease with minimal clinical expression unlinked to the PKD1 locusG D Wright, A E Hughes, K A Larkin, et al.
Human Genetics|January 1, 1981
Detection of cystic fibrosis homozygotes and heterozygotes by serum isoelectrofocusingG B Nevin, N C Nevin, A O Redmond, et al.
British Journal of Obstetrics and Gynaecology|March 21, 1998
Transplacental early amniocentesis and pregnancy outcomeS Tharmaratnam, S Sadek, E K Steele, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Contiguous gene deletion syndrome involving glycerol kinase and Duchenne muscular dystrophy lociM Asghar, N C Nevin, E D Beattie, et al.
Human Mutation|January 1, 1995
Three novel mutations in the EGF precursor homology domain of the low-density lipoprotein receptor gene in Northern Irish patients with familial hypercholesterolemiaA J Ward, M O'Kane, I Young, et al.
Pageof 23