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December 1993 (Volume 30, Number 12). [Index by author]

		Book Review Editor's Note Research Article

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Book Review

Heredity and Your Family's Health
Hilary J Harris
J Med Genet 1993; 30: 1043. doi:10.1136/jmg.30.12.1043 [PDF] [Request Permissions]

Editor's Note

Journal of Medical Genetics: Cytogenetics Editor
Peter S Harper
J Med Genet 1993; 30: 1043. doi:10.1136/jmg.30.12.1043-a [PDF] [Request Permissions]

Research Article

A specific mutation for Huntington's disease.
P S Harper
J Med Genet 1993; 30: 975-977. doi:10.1136/jmg.30.12.975 [PDF] [Request Permissions]

Dynamic mutations on the move.
G R Sutherland and R I Richards
J Med Genet 1993; 30: 978-981. doi:10.1136/jmg.30.12.978 [PDF] [Request Permissions]

Gametic but not somatic instability of CAG repeat length in Huntington's disease.
M E MacDonald, G Barnes, J Srinidhi, M P Duyao, C M Ambrose, R H Myers, J Gray, P M Conneally, A Young, and J Penney
J Med Genet 1993; 30: 982-986. doi:10.1136/jmg.30.12.982 [Abstract] [PDF] [Request Permissions]

Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.
Y P Goldberg, S E Andrew, J Theilmann, B Kremer, F Squitieri, H Telenius, J D Brown, and M R Hayden
J Med Genet 1993; 30: 987-990. doi:10.1136/jmg.30.12.987 [Abstract] [PDF] [Request Permissions]

Molecular analysis of late onset Huntington's disease.
B Kremer, F Squitieri, H Telenius, S E Andrew, J Theilmann, N Spence, Y P Goldberg, and M R Hayden
J Med Genet 1993; 30: 991-995. doi:10.1136/jmg.30.12.991 [Abstract] [PDF] [Request Permissions]

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
K E De Rooij, P A De Koning Gans, M I Skraastad, R D Belfroid, M Vegter-Van Der Vlis, R A Roos, E Bakker, G J Van Ommen, J T Den Dunnen, and M Losekoot
J Med Genet 1993; 30: 996-1002. doi:10.1136/jmg.30.12.996 [Abstract] [PDF] [Request Permissions]

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.
L H Barron, J P Warner, M Porteous, S Holloway, S Simpson, R Davidson, and D J Brock
J Med Genet 1993; 30: 1003-1007. doi:10.1136/jmg.30.12.1003 [Abstract] [PDF] [Request Permissions]

Mutation size and age at onset in Huntington's disease.
D Craufurd and A Dodge
J Med Genet 1993; 30: 1008-1011. doi:10.1136/jmg.30.12.1008 [Abstract] [PDF] [Request Permissions]

Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.
J C MacMillan, P J Morrison, N C Nevin, D J Shaw, P S Harper, O W Quarrell, and R G Snell
J Med Genet 1993; 30: 1012-1013. doi:10.1136/jmg.30.12.1012 [Abstract] [PDF] [Request Permissions]

Huntington's disease in Grampian region: correlation of the CAG repeat number and the age of onset of the disease.
S A Simpson, M J Davidson, and L H Barron
J Med Genet 1993; 30: 1014-1017. doi:10.1136/jmg.30.12.1014 [Abstract] [PDF] [Request Permissions]

Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland.
P J Morrison, C A Graham, and N C Nevin
J Med Genet 1993; 30: 1018-1019. doi:10.1136/jmg.30.12.1018 [Abstract] [PDF] [Request Permissions]

Presymptomatic testing for Huntington's disease: a world wide survey. The World Federation of Neurology Research Group on Huntington's Disease.
J Med Genet 1993; 30: 1020-1022. doi:10.1136/jmg.30.12.1020 [Abstract] [PDF] [Request Permissions]

Attitudes of neurologists, psychiatrists, and psychotherapists towards predictive testing for Huntington's disease in Germany.
U Thies, B Bockel, and V Bochdalofsky
J Med Genet 1993; 30: 1023-1027. doi:10.1136/jmg.30.12.1023 [Abstract] [PDF] [Request Permissions]

Ethical and social issues in presymptomatic testing for Huntington's disease: a European Community collaborative study. European Community Huntington's Disease Collaborative Study Group.
J Med Genet 1993; 30: 1028-1035. doi:10.1136/jmg.30.12.1028 [Abstract] [PDF] [Request Permissions]

Predictive testing for Huntington's disease: after the gene. The United Kingdom Huntington's Disease Prediction Consortium.
S A Simpson and A E Harding
J Med Genet 1993; 30: 1036-1038. doi:10.1136/jmg.30.12.1036 [Abstract] [PDF] [Request Permissions]

15th International World Federation of Neurology Workshop on Huntington's Disease, 31 August-3 September 1993, Boston, Massachusetts, USA.
J C MacMillan and N P Quinn
J Med Genet 1993; 30: 1039-1041. doi:10.1136/jmg.30.12.1039 [PDF] [Request Permissions]

George Huntington: the man behind the eponym.
R M van der Weiden
J Med Genet 1993; 30: 1042. doi:10.1136/jmg.30.12.1042 [PDF] [Request Permissions]

DNA storage and duplicate sampling: lessons learnt from testing for Huntington's disease.
P J Morrison, C A Graham, and N C Nevin
J Med Genet 1993; 30: 1042. doi:10.1136/jmg.30.12.1042-a [PDF] [Request Permissions]

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.
I A Glass, P Good, M P Coleman, P Fullwood, M G Giles, S Lindsay, A H Nemeth, K E Davies, H A Willshaw, and A Fielder
J Med Genet 1993; 30: 1044-1050. doi:10.1136/jmg.30.12.1044 [Abstract] [PDF] [Request Permissions]

Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting.
Y L Zheng, N P Carter, C M Price, S M Colman, P J Milton, G A Hackett, M F Greaves, and M A Ferguson-Smith
J Med Genet 1993; 30: 1051-1056. doi:10.1136/jmg.30.12.1051 [Abstract] [PDF] [Request Permissions]

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	Heredity and Your Family's Health Hilary J Harris J Med Genet 1993; 30: 1043. doi:10.1136/jmg.30.12.1043 [PDF] [Request Permissions]

	Journal of Medical Genetics: Cytogenetics Editor Peter S Harper J Med Genet 1993; 30: 1043. doi:10.1136/jmg.30.12.1043-a [PDF] [Request Permissions]

	A specific mutation for Huntington's disease. P S Harper J Med Genet 1993; 30: 975-977. doi:10.1136/jmg.30.12.975 [PDF] [Request Permissions]

	Dynamic mutations on the move. G R Sutherland and R I Richards J Med Genet 1993; 30: 978-981. doi:10.1136/jmg.30.12.978 [PDF] [Request Permissions]

	Gametic but not somatic instability of CAG repeat length in Huntington's disease. M E MacDonald, G Barnes, J Srinidhi, M P Duyao, C M Ambrose, R H Myers, J Gray, P M Conneally, A Young, and J Penney J Med Genet 1993; 30: 982-986. doi:10.1136/jmg.30.12.982 [Abstract] [PDF] [Request Permissions]

	Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases. Y P Goldberg, S E Andrew, J Theilmann, B Kremer, F Squitieri, H Telenius, J D Brown, and M R Hayden J Med Genet 1993; 30: 987-990. doi:10.1136/jmg.30.12.987 [Abstract] [PDF] [Request Permissions]

	Molecular analysis of late onset Huntington's disease. B Kremer, F Squitieri, H Telenius, S E Andrew, J Theilmann, N Spence, Y P Goldberg, and M R Hayden J Med Genet 1993; 30: 991-995. doi:10.1136/jmg.30.12.991 [Abstract] [PDF] [Request Permissions]

	Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range. K E De Rooij, P A De Koning Gans, M I Skraastad, R D Belfroid, M Vegter-Van Der Vlis, R A Roos, E Bakker, G J Van Ommen, J T Den Dunnen, and M Losekoot J Med Genet 1993; 30: 996-1002. doi:10.1136/jmg.30.12.996 [Abstract] [PDF] [Request Permissions]

	A study of the Huntington's disease associated trinucleotide repeat in the Scottish population. L H Barron, J P Warner, M Porteous, S Holloway, S Simpson, R Davidson, and D J Brock J Med Genet 1993; 30: 1003-1007. doi:10.1136/jmg.30.12.1003 [Abstract] [PDF] [Request Permissions]

	Mutation size and age at onset in Huntington's disease. D Craufurd and A Dodge J Med Genet 1993; 30: 1008-1011. doi:10.1136/jmg.30.12.1008 [Abstract] [PDF] [Request Permissions]

	Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea. J C MacMillan, P J Morrison, N C Nevin, D J Shaw, P S Harper, O W Quarrell, and R G Snell J Med Genet 1993; 30: 1012-1013. doi:10.1136/jmg.30.12.1012 [Abstract] [PDF] [Request Permissions]

	Huntington's disease in Grampian region: correlation of the CAG repeat number and the age of onset of the disease. S A Simpson, M J Davidson, and L H Barron J Med Genet 1993; 30: 1014-1017. doi:10.1136/jmg.30.12.1014 [Abstract] [PDF] [Request Permissions]

	Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland. P J Morrison, C A Graham, and N C Nevin J Med Genet 1993; 30: 1018-1019. doi:10.1136/jmg.30.12.1018 [Abstract] [PDF] [Request Permissions]

	Presymptomatic testing for Huntington's disease: a world wide survey. The World Federation of Neurology Research Group on Huntington's Disease. J Med Genet 1993; 30: 1020-1022. doi:10.1136/jmg.30.12.1020 [Abstract] [PDF] [Request Permissions]

	Attitudes of neurologists, psychiatrists, and psychotherapists towards predictive testing for Huntington's disease in Germany. U Thies, B Bockel, and V Bochdalofsky J Med Genet 1993; 30: 1023-1027. doi:10.1136/jmg.30.12.1023 [Abstract] [PDF] [Request Permissions]

	Ethical and social issues in presymptomatic testing for Huntington's disease: a European Community collaborative study. European Community Huntington's Disease Collaborative Study Group. J Med Genet 1993; 30: 1028-1035. doi:10.1136/jmg.30.12.1028 [Abstract] [PDF] [Request Permissions]

	Predictive testing for Huntington's disease: after the gene. The United Kingdom Huntington's Disease Prediction Consortium. S A Simpson and A E Harding J Med Genet 1993; 30: 1036-1038. doi:10.1136/jmg.30.12.1036 [Abstract] [PDF] [Request Permissions]

	15th International World Federation of Neurology Workshop on Huntington's Disease, 31 August-3 September 1993, Boston, Massachusetts, USA. J C MacMillan and N P Quinn J Med Genet 1993; 30: 1039-1041. doi:10.1136/jmg.30.12.1039 [PDF] [Request Permissions]

	George Huntington: the man behind the eponym. R M van der Weiden J Med Genet 1993; 30: 1042. doi:10.1136/jmg.30.12.1042 [PDF] [Request Permissions]

	DNA storage and duplicate sampling: lessons learnt from testing for Huntington's disease. P J Morrison, C A Graham, and N C Nevin J Med Genet 1993; 30: 1042. doi:10.1136/jmg.30.12.1042-a [PDF] [Request Permissions]

	Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome. I A Glass, P Good, M P Coleman, P Fullwood, M G Giles, S Lindsay, A H Nemeth, K E Davies, H A Willshaw, and A Fielder J Med Genet 1993; 30: 1044-1050. doi:10.1136/jmg.30.12.1044 [Abstract] [PDF] [Request Permissions]

	Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting. Y L Zheng, N P Carter, C M Price, S M Colman, P J Milton, G A Hackett, M F Greaves, and M A Ferguson-Smith J Med Genet 1993; 30: 1051-1056. doi:10.1136/jmg.30.12.1051 [Abstract] [PDF] [Request Permissions]