Found: 17
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Identification of single nucleotide polymorphisms in FOXJ1 and their association with allergic rhinitis.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 4, p. 292, doi. 10.1007/s10038-006-0359-8
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- Article
Resequencing of the characterised CTGF gene to identify novel or known variants, and analysis of their association with diabetic nephropathy.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 383, doi. 10.1007/s10038-006-0368-7
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- Article
The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 298, doi. 10.1007/s10038-006-0361-1
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- Article
An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 284, doi. 10.1007/s10038-005-0358-1
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- Article
Detection of novel Y SNPs provides further insights into Y chromosomal variation in Pakistan.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 375, doi. 10.1007/s10038-005-0357-2
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- Article
Microarray analysis of promoter methylation in lung cancers.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 368, doi. 10.1007/s10038-005-0355-4
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- Article
Unified method for Bayesian calculation of genetic risk.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 387, doi. 10.1007/s10038-006-0371-z
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- Article
A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 379, doi. 10.1007/s10038-006-0360-2
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- Article
Ancient retroviral insertions among human populations.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 353, doi. 10.1007/s10038-006-0370-0
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- Article
TCR variable gene involvement in chromosome inversion between 14q11 and 14q24 in adult T-cell leukemia.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 326, doi. 10.1007/s10038-006-0364-y
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- Article
Fifty years of genetic epidemiology, with special reference to Japan.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 269, doi. 10.1007/s10038-006-0366-9
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- Article
The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 305, doi. 10.1007/s10038-006-0362-0
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- Article
Estimation of haplotype associated with several quantitative phenotypes based on maximization of area under a receiver operating characteristic (ROC) curve.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 314, doi. 10.1007/s10038-006-0363-z
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- Article
Corrective effect on Fabry mice of yeast recombinant human α-galactosidase with N-linked sugar chains suitable for lysosomal delivery.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 341, doi. 10.1007/s10038-006-0369-6
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- Article
MTHFR C677T and A1298C polymorphisms are risk factors for Down’s syndrome in Indian mothers.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 278, doi. 10.1007/s10038-005-0356-3
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- Article
Mutations of the puratrophin-1 ( PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 363, doi. 10.1007/s10038-006-0372-y
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- Article
Molecular characterization of a novel translocation t(5;14)(q21;q32) in a patient with congenital abnormalities.
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- Journal of Human Genetics, 2006, v. 51, n. 4, p. 335, doi. 10.1007/s10038-006-0365-x
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- Article