Found: 14
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Linkage to the 8p21.1 Region Including the CLU Gene in Age at Onset Stratified Alzheimer's Disease Families.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 23, n. 1, p. 13, doi. 10.3233/JAD-2010-101359
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- Article
Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 649, doi. 10.1038/jhg.2010.79
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- Article
Genome scan of Alzheimer families stratified for age at onset reveals linkage to the CLU gene in 8p21.1
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- 2010
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- Abstract
Fine mapping in 20p13 with families having a mixed phenotype of Alzheimer's disease and vascular dementia
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- 2010
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- Abstract
Linkage analysis on autopsy-confirmed familial Alzheimer's disease supports an Alzheimer locus in 8q24
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- 2010
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- Abstract
P1-351: Two genome scans on Swedish families with Alzheimer’s disease and other dementias
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- 2006
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- Abstract
P1-351: Two genome scans on Swedish families with Alzheimer’s disease and other dementias
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- 2006
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- Abstract
Linkage Analysis of Autopsy-Confirmed Familial Alzheimer Disease Supports an Alzheimer Disease Locus in 8q24.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2011, v. 31, n. 2, p. 109, doi. 10.1159/000323808
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- Article
Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease.
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- European Journal of Human Genetics, 2008, v. 16, n. 2, p. 202, doi. 10.1038/sj.ejhg.5201946
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- Article
The use of grid computing to drive data-intensive genetic research.
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- European Journal of Human Genetics, 2007, v. 15, n. 6, p. 694, doi. 10.1038/sj.ejhg.5201815
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- Article
Brain-derived neurotrophic factor gene variation influences cerebrospinal fluid 3-methoxy-4-hydroxyphenylglycol concentrations in healthy volunteers.
- Published in:
- Journal of Neural Transmission, 2008, v. 115, n. 12, p. 1695, doi. 10.1007/s00702-008-0113-9
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- Article
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome.
- Published in:
- Human Mutation, 1998, v. 12, n. 6, p. 377, doi. 10.1002/(SICI)1098-1004(1998)12:6<377::AID-HUMU3>3.0.CO;2-I
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- Article
A novel mutation (C201R) in the transmembrane domain of connexin 32 in severe x-linked charcot-marie-tooth disease.
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- Human Mutation, 1998, v. 11, p. S8, doi. 10.1002/humu.1380110104
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- Article
Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1.
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- Human Heredity, 1995, v. 45, n. 3, p. 121, doi. 10.1159/000154272
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- Article