Works matching IS 03406717 AND DT 2004 AND VI 115 AND IP 3
Results: 16
Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage.
- Published in:
- Human Genetics, 2004, v. 115, n. 3, p. 255
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- Article
Qualitative and quantitative analysis of the effect of splicing mutations in propionic acidemia underlying non-severe phenotypes.
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- Human Genetics, 2004, v. 115, n. 3, p. 239, doi. 10.1007/s00439-004-1147-1
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Max Perutz (ed) I wish I’d make you angry earlier. Expanded edition (2003): Cold Spring Harbor Laboratory Press, ISBN 0-87969-674-5, paperback, £11.00.
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- Human Genetics, 2004, v. 115, n. 3, p. 267
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B. Wissinger, S. Kohl, U. Langenbeck (eds): Developments in ophthalmology vol 37: Genetics in ophthalmology: S. Karger AG, ISBN 8-8055-7578-5, hardcover, 160.00 Euros, 224 pages.
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- Human Genetics, 2004, v. 115, n. 3, p. 264, doi. 10.1007/s00439-004-1150-6
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Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data.
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- Human Genetics, 2004, v. 115, n. 3, p. 221, doi. 10.1007/s00439-004-1130-x
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Thomas von Zglinicki (ed) Aging at the molecular level (2003): Kluwer Academic Publishers, Dordrecht, Boston, London, ISBN 1-4020-1738-3, hardcover, 125.00 Euro, $138.00.
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- Human Genetics, 2004, v. 115, n. 3, p. 268, doi. 10.1007/s00439-004-1159-x
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Alan E. Guttmacher, Francis S. Collins, Jeffrey M. Drazen (eds): Genomic medicine: articles from the New England Journal of Medicine: Johns Hopkins University Press (2004), The New England Journal of Medicine, ISBN 0-8018-7979-5, paperback, £27.50.
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- Human Genetics, 2004, v. 115, n. 3, p. 265
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A resistin gene polymorphism is associated with body mass index in women.
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- Human Genetics, 2004, v. 115, n. 3, p. 208
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Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene.
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- Human Genetics, 2004, v. 115, n. 3, p. 185
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Mono-nucleotide repeats (MNRs): a neglected polymorphism for generating high density genetic maps in silico.
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- Human Genetics, 2004, v. 115, n. 3, p. 213, doi. 10.1007/s00439-004-1135-5
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Chromosome 17p12-q11 harbors susceptibility loci for systemic lupus erythematosus.
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- Human Genetics, 2004, v. 115, n. 3, p. 230
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Identification of a novel type 1 diabetes susceptibility gene, T-bet.
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- Human Genetics, 2004, v. 115, n. 3, p. 177, doi. 10.1007/s00439-004-1146-2
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- Article
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.
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- Human Genetics, 2004, v. 115, n. 3, p. 248, doi. 10.1007/s00439-004-1143-5
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- Article
Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.
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- Human Genetics, 2004, v. 115, n. 3, p. 191
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- Article
Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis.
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- Human Genetics, 2004, v. 115, n. 3, p. 200, doi. 10.1007/s00439-004-1151-5
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- Article
Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination.
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- Human Genetics, 2004, v. 115, n. 3, p. 263
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- Article