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Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

http://www.wikidata.org/entity/Q33734010

about

Incidence and mutation rates of Huntington's disease in Spain: experience of 9 years of direct genetic testing.Evidence from biomarkers and surrogate endpoints.What do we know about Late Onset Huntington's Disease?

P2860

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P2860

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

http://www.wikidata.org/entity/Q33734010

description

1995 nî lūn-bûn

@nan

1995 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1995 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

1995年の論文

@ja

1995年論文

@yue

1995年論文

@zh-hant

1995年論文

@zh-hk

1995年論文

@zh-mo

1995年論文

@zh-tw

1995年论文

@wuu

name

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@ast

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@en

type

label

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@ast

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@en

prefLabel

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@ast

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@en

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P1433

Journal of Neurology, Neurosurgery and Psychiatry

P1476

Molecular diagnostic analysis for Huntington's disease: a prospective evaluation.

@en

P2093

Davies P

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Harper PS

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MacMillan JC

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P2860

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

Expanded CAG trinucleotide repeat of Huntington's disease gene in a patient with schizophrenia and normal striatal histology.

Trinucleotide repeat length instability and age of onset in Huntington's disease.

Presymptomatic testing for Huntington's disease in the United Kingdom. The United Kingdom Huntington's Disease Prediction Consortium

Huntington disease without CAG expansion: phenocopies or errors in assignment?

Proceed with care: direct predictive testing for Huntington disease.

Mutation analysis in patients with possible but apparently sporadic Huntington's disease.

Molecular analysis and clinical correlations of the Huntington's disease mutation.

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.

P304

496-498

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scholarly article

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10.1136/JNNP.58.4.496

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4

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58

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1995-04-01T00:00:00Z

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15459756

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7738566

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Huntington disease

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1073445

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