Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 9
Results: 17
Polymorphisms in interleukin 8 and its receptors ( IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 781, doi. 10.1007/s10038-006-0021-5
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Functional analysis of PKHD1 splicing in autosomal recessive polycystic kidney disease.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 788, doi. 10.1007/s10038-006-0022-4
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- Article
Refinement of the locus for autosomal recessive cone–rod dystrophy (CORD8) linked to chromosome 1q23–q24 in a Pakistani family and exclusion of candidate genes.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 827, doi. 10.1007/s10038-006-0028-y
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Frequent DAP kinase but not p14 or Apaf-1 hypermethylation in B-cell chronic lymphocytic leukemia.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 832, doi. 10.1007/s10038-006-0029-x
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Longevity-associated NADH dehydrogenase subunit-2 237 Leu/Met polymorphism influences the effects of alcohol consumption on serum uric acid levels in nonobese Japanese men.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 765, doi. 10.1007/s10038-006-0018-0
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An algorithm for model construction and its applications to pharmacogenomic studies.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 751, doi. 10.1007/s10038-006-0016-2
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A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 760, doi. 10.1007/s10038-006-0017-1
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Study of AZFc partial deletion gr/gr in fertile and infertile Japanese males.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 794, doi. 10.1007/s10038-006-0024-2
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Pure de-novo 5 Mb duplication at Xp11.22–p11.23 in a male: phenotypic and molecular characterization.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 815, doi. 10.1007/s10038-006-0023-3
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Pharmacogenetic determinants of variability in lipid-lowering response to pravastatin therapy.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 822, doi. 10.1007/s10038-006-0025-1
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The confidence interval of allelic odds ratios under the Hardy–Weinberg disequilibrium.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 772, doi. 10.1007/s10038-006-0020-6
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Unique origin of Andaman Islanders: insight from autosomal loci.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 800, doi. 10.1007/s10038-006-0026-0
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Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 805, doi. 10.1007/s10038-006-0027-z
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Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuoles.
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- 2006
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- Correction Notice
Role of B cell inhibitory receptor polymorphisms in systemic lupus erythematosus: a negative times a negative makes a positive.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 741, doi. 10.1007/s10038-006-0030-4
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Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa.
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- 2006
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- Correction Notice
Farber lipogranulomatosis: clinical and molecular genetic analysis reveals a novel mutation in an Indian family.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 811, doi. 10.1007/s10038-006-0019-z
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- Article