Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease-Reference-Cited by-同舟云学术

Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease

Published:1991-06 Issue:2 Volume:87 Page:159-161
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Pulst S. -M.,Fain P.,Cohn V.,Nee L. E.,Polinsky R. J.,Korenberg J. R.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00204173.pdf

Reference17 articles.

1. Goate AM, et al (1989) Predisposing locus for Alzheimer's disease on chromosome 21. Lancet I:352?355

2. Katzman R (1986) Alzheimer's disease. N Eng J Med 314:964?973

3. Lathrop GM, Lalouel JM, Julier C, Ott J (1985) Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 37:482?498

4. Nee LE, Polinsky RJ, Eldridge R, Weingartner H, Smallberg S, Ebert M (1983) A family with histologically confirmed Alzheimer's disease Arch Neurol 40:203?208

5. NIA Catalogue of Cell Lines (1989) US Department of Health and Human Services, Public Health Service, Bethesda, Md

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1. Potassium channel dysfunction in fibroblasts identifies patients with Alzheimer disease.;Proceedings of the National Academy of Sciences;1993-09-01

2. Linkage of familial alzheimer disease to chromosome 14 in two large early-onset pedigrees: Effects of marker allele frequencies on lod scores;American Journal of Medical Genetics;1993-05-01

3. Locus Heterogeneity of Alzheimer’s Disease;Research and Perspectives in Alzheimer’s Disease;1992

4. Report of the committee on clinical disorders, chromosome aberrations and uniparental disomy;Cytogenetic and Genome Research;1991