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P L Pearson

Showing results (191-200 of 211) with videos related to

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Genomics|April 1, 1988
Two different genes for X-linked retinitis pigmentosaB Wirth, M J Denton, J D Chen, et al.
Nucleic Acids Research|July 25, 1989
High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridizationL A Blonden, J T den Dunnen, H M van Paassen, et al.
Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.
Diabetologia|June 16, 2000
The exon 16-3t variant of the sulphonylurea receptor gene is not a risk factor for Type II diabetes mellitus in the Dutch Breda cohortJ H van Tilburg, L B Rozeman, H van Someren, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16pJ G Dauwerse, T Kievits, G C Beverstock, et al.
Neurology|December 25, 2003
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyB P C van de Warrenburg, D S Verbeek, S J Piersma, et al.
Genes and Immunity|March 12, 2004
Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patientsM J van Belzen, B P C Koeleman, J B A Crusius, et al.
American Journal of Human Genetics|December 1, 1989
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplicationsJ T Den Dunnen, P M Grootscholten, E Bakker, et al.
European Journal of Clinical Investigation|March 27, 1999
Management of renal cell carcinoma in von Hippel-Lindau diseaseF J Hes, P J Slootweg, T J van Vroonhoven, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
Anticipation in familial intracranial aneurysms in consecutive generationsP M Struycken, G Pals, M Limburg, et al.
Pageof 22

Showing results (191-200 of 211) with videos related to

Sort By:
Pageof 22
Genomics|April 1, 1988
Two different genes for X-linked retinitis pigmentosaB Wirth, M J Denton, J D Chen, et al.
Nucleic Acids Research|July 25, 1989
High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridizationL A Blonden, J T den Dunnen, H M van Paassen, et al.
Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.
Diabetologia|June 16, 2000
The exon 16-3t variant of the sulphonylurea receptor gene is not a risk factor for Type II diabetes mellitus in the Dutch Breda cohortJ H van Tilburg, L B Rozeman, H van Someren, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16pJ G Dauwerse, T Kievits, G C Beverstock, et al.
Neurology|December 25, 2003
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyB P C van de Warrenburg, D S Verbeek, S J Piersma, et al.
Genes and Immunity|March 12, 2004
Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patientsM J van Belzen, B P C Koeleman, J B A Crusius, et al.
American Journal of Human Genetics|December 1, 1989
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplicationsJ T Den Dunnen, P M Grootscholten, E Bakker, et al.
European Journal of Clinical Investigation|March 27, 1999
Management of renal cell carcinoma in von Hippel-Lindau diseaseF J Hes, P J Slootweg, T J van Vroonhoven, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
Anticipation in familial intracranial aneurysms in consecutive generationsP M Struycken, G Pals, M Limburg, et al.
Pageof 22