Works matching IS 03406717 AND DT 2011 AND VI 129 AND IP 5
Results: 13
Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.
- Published in:
- Human Genetics, 2011, v. 129, n. 5, p. 497, doi. 10.1007/s00439-011-0947-3
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- Article
Genes in the insulin and insulin-like growth factor pathway and odds of metachronous colorectal neoplasia.
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- Human Genetics, 2011, v. 129, n. 5, p. 503, doi. 10.1007/s00439-010-0942-0
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- Article
Maternal de novo triple mosaicism for two single OCRL nucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome family.
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- Human Genetics, 2011, v. 129, n. 5, p. 513, doi. 10.1007/s00439-010-0944-y
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- Article
Genomic and genealogical investigation of the French Canadian founder population structure.
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- Human Genetics, 2011, v. 129, n. 5, p. 521, doi. 10.1007/s00439-010-0945-x
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- Article
A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.
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- Human Genetics, 2011, v. 129, n. 5, p. 487, doi. 10.1007/s00439-010-0937-x
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- Article
A genome-wide screen of gene-gene interactions for rheumatoid arthritis susceptibility.
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- Human Genetics, 2011, v. 129, n. 5, p. 473, doi. 10.1007/s00439-010-0943-z
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- Article
Transcriptional control of the human glucocorticoid receptor: identification and analysis of alternative promoter regions.
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- Human Genetics, 2011, v. 129, n. 5, p. 533, doi. 10.1007/s00439-011-0949-1
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- Article
BR-squared: a practical solution to the winner's curse in genome-wide scans.
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- Human Genetics, 2011, v. 129, n. 5, p. 545, doi. 10.1007/s00439-011-0948-2
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- Article
Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients
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- Human Genetics, 2011, v. 129, n. 5, p. 553, doi. 10.1007/s00439-011-0954-4
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- Article
Genetic analysis of biological pathway data through genomic randomization.
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- Human Genetics, 2011, v. 129, n. 5, p. 563, doi. 10.1007/s00439-011-0956-2
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- Article
Mutations in Fanconi anemia genes and the risk of esophageal cancer.
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- Human Genetics, 2011, v. 129, n. 5, p. 573, doi. 10.1007/s00439-011-0951-7
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- Article
Jane Gitschier: Speaking of genetics. A collection of interviews.
- Published in:
- 2011
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- Publication type:
- Book Review
Recent progress in the study of the genetics of height.
- Published in:
- Human Genetics, 2011, v. 129, n. 5, p. 465, doi. 10.1007/s00439-011-0969-x
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- Publication type:
- Article