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O W Quarrell

Showing results (21-30 of 35) with videos related to

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Clinical Genetics|March 1, 1988
Population studies of Huntington's disease in WalesO W Quarrell, A Tyler, M P Jones, et al.
Journal of Medical Genetics|August 1, 1990
Exclusion testing in pregnancy for Huntington's diseaseA Tyler, O W Quarrell, L P Lazarou, et al.
Journal of Medical Genetics|April 1, 1995
Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphismD T Pilz, A Dalton, A Long, et al.
Lancet (London, England)|June 6, 1987
Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerO W Quarrell, A L Meredith, A Tyler, et al.
Human Molecular Genetics|December 1, 1996
ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndromeD J Picketts, D R Higgs, S Bachoo, et al.
Journal of Medical Genetics|April 1, 1991
Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndromeO W Quarrell, R G Snell, M A Curtis, et al.
American Journal of Human Genetics|July 1, 1990
Ethical and legal dilemmas arising during predictive testing for adult-onset disease: the experience of Huntington diseaseM Huggins, M Bloch, S Kanani, et al.
Journal of Medical Genetics|November 1, 1989
Linkage disequilibrium in Huntington's disease: an improved localisation for the geneR G Snell, L P Lazarou, S Youngman, 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.
Journal of Medical Genetics|May 1, 1995
Genetic linkage analysis in hereditary non-polyposis colon cancer syndromeN J Froggatt, J Koch, R Davies, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Clinical Genetics|March 1, 1988
Population studies of Huntington's disease in WalesO W Quarrell, A Tyler, M P Jones, et al.
Journal of Medical Genetics|August 1, 1990
Exclusion testing in pregnancy for Huntington's diseaseA Tyler, O W Quarrell, L P Lazarou, et al.
Journal of Medical Genetics|April 1, 1995
Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphismD T Pilz, A Dalton, A Long, et al.
Lancet (London, England)|June 6, 1987
Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerO W Quarrell, A L Meredith, A Tyler, et al.
Human Molecular Genetics|December 1, 1996
ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndromeD J Picketts, D R Higgs, S Bachoo, et al.
Journal of Medical Genetics|April 1, 1991
Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndromeO W Quarrell, R G Snell, M A Curtis, et al.
American Journal of Human Genetics|July 1, 1990
Ethical and legal dilemmas arising during predictive testing for adult-onset disease: the experience of Huntington diseaseM Huggins, M Bloch, S Kanani, et al.
Journal of Medical Genetics|November 1, 1989
Linkage disequilibrium in Huntington's disease: an improved localisation for the geneR G Snell, L P Lazarou, S Youngman, 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.
Journal of Medical Genetics|May 1, 1995
Genetic linkage analysis in hereditary non-polyposis colon cancer syndromeN J Froggatt, J Koch, R Davies, et al.
Pageof 4