Works matching IS 03406717 AND DT 2004 AND VI 114 AND IP 6
Results: 14
Microarray Gene Expression Data Analysis: A Beginners Guide: Helen C. Causton, John Quackenbush, Alvis Brazma (Editors), Blackwell, 2003, ISBN 1-4051-0682-4, paperback, 160 pages, £34.99.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
The Genetic Basis of Common Diseases, 2nd Edition: R.A. King, J.I. Rotter, A.G. Motulsky (Editors), Oxford University Press, 2002, ISBN 0-1951-2582-7, hardcover, £145.00.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Genetics of Movement Disorders: Stephan-M. Pulst (Editor), Harcourt Publishers, 2002, ISBN 0-1256-6652-7, hardcover, £86.00.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 541, doi. 10.1007/s00439-004-1114-x
- By:
- Publication type:
- Article
Mutations.
- Published in:
- 2004
- Publication type:
- Table of Contents
Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 573, doi. 10.1007/s00439-004-1095-9
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- Publication type:
- Article
Fine mapping a gene for pediatric gastroesophageal reflux on human chromosome 13q14.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 562, doi. 10.1007/s00439-004-1096-8
- By:
- Publication type:
- Article
Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 534, doi. 10.1007/s00439-004-1100-3
- By:
- Publication type:
- Article
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 527, doi. 10.1007/s00439-004-1102-1
- By:
- Publication type:
- Article
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 553, doi. 10.1007/s00439-004-1104-z
- By:
- Publication type:
- Article
Parents of children with autosomal recessive diseases are not always carriers of the respective mutant alleles.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 521, doi. 10.1007/s00439-004-1105-y
- By:
- Publication type:
- Article
Variants of CYP46A1 may interact with age and APOE to influence CSF Aβ42 levels in Alzheimer’s disease.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 581, doi. 10.1007/s00439-004-1107-9
- By:
- Publication type:
- Article
Quasi-linkage: a confounding factor in linkage analysis of complex diseases?
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 588, doi. 10.1007/s00439-004-1109-7
- By:
- Publication type:
- Article
Fine mapping of the Schnyder’s crystalline corneal dystrophy locus.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 594, doi. 10.1007/s00439-004-1110-1
- By:
- Publication type:
- Article