Family history and DNA analysis in patients with suspected Huntington's disease. - Wikidata - wikimedia - TriplyDB

Family history and DNA analysis in patients with suspected Huntington's disease.

Family history and DNA analysis in patients with suspected Huntington's disease.

http://www.wikidata.org/entity/Q35458053

about

High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia.Neuronal intranuclear and neuropil inclusions for pathological assessment of Huntington's disease.Clinical and genetic investigation of a Brazilian family with Huntington's disease.HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.Huntington's disease in Greece: the experience of 14 years.Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.The Impact of Family History on the Clinical Features of Huntington's Disease.

P2860

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P2860

Family history and DNA analysis in patients with suspected Huntington's disease.

http://www.wikidata.org/entity/Q35458053

description

2000 nî lūn-bûn

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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

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2000年论文

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name

Family history and DNA analysis in patients with suspected Huntington's disease.

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Family history and DNA analysis in patients with suspected Huntington's disease.

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type

label

Family history and DNA analysis in patients with suspected Huntington's disease.

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Family history and DNA analysis in patients with suspected Huntington's disease.

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prefLabel

Family history and DNA analysis in patients with suspected Huntington's disease.

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Family history and DNA analysis in patients with suspected Huntington's disease.

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P1433

Journal of Neurology, Neurosurgery and Psychiatry

P1476

Family history and DNA analysis in patients with suspected Huntington's disease.

@en

P2093

Belfroid RD

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Kremer HP

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Losekoot M

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Maat-Kievit JA

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Roos RA

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Siesling S

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Vegter-van de Vlis M

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P2860

Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping

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

Molecular analysis of late onset Huntington's disease.

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

Age at onset in Huntington's disease: effect of line of inheritance and patient's sex.

Late onset of Huntington's disease

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

Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia

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

P304

54-59

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10.1136/JNNP.69.1.54

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1

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69

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12453417

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P698

10864604

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P921

Huntington disease

nucleic acid sequence analysis

P932

1737014

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