(Q53187559)

12 May 2018

title

Predisposing locus for Alzheimer's disease on chromosome 21. (English)

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12 May 2018

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A M Goate

1

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12 May 2018

A R Haynes

2

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12 May 2018

M J Owen

3

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12 May 2018

M Farrall

4

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12 May 2018

L A James

5

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12 May 2018

L Y Lai

6

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12 May 2018

M J Mullan

7

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12 May 2018

P Roques

8

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12 May 2018

M N Rossor

9

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12 May 2018

R Williamson

10

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12 May 2018

language of work or name

English

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publication date

1 February 1989

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12 May 2018

published in

The Lancet

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12 May 2018

volume

1

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12 May 2018

page(s)

352-355

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12 May 2018

issue

8634

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12 May 2018

Dementia of the Alzheimer type. Clinical genetics, natural history, and associated conditions

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Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome.

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The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

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A giant locus for the Duchenne and Becker muscular dystrophy gene

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Absence of Linkage of Chromosome 21q21 Markers to Familial Alzheimer's Disease

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Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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Genetic linkage map of human chromosome 21

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Strategies for multilocus linkage analysis in humans

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The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene.

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Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus.

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Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families.

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Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect.

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10.1016/S0140-6736(89)91725-X

Identifiers

DOI

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12 May 2018

PubMed ID

2563508

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12 May 2018