Works matching IS 1434-5161 AND VI 52 AND IP 7 AND DT 2007
Results: 9
Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 607, doi. 10.1007/s10038-007-0163-0
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- Article
Testing the hypothesis of an ancient Roman soldier origin of the Liqian people in northwest China: a Y-chromosome perspective.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 584, doi. 10.1007/s10038-007-0155-0
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- Article
A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 °C.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 599, doi. 10.1007/s10038-007-0157-y
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Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn’s disease in Japanese patients.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 575, doi. 10.1007/s10038-007-0156-z
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- Article
Allelic variation in the NPY gene in 14 Indian populations.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 592, doi. 10.1007/s10038-007-0158-x
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- Article
The Tol1 transposable element of the medaka fish moves in human and mouse cells.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 628, doi. 10.1007/s10038-007-0161-2
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- Article
Three novel mutations of the PAX6 gene in Japanese aniridia patients.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 571, doi. 10.1007/s10038-007-0153-2
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- Article
Association of the HTRA1 gene variant with age-related macular degeneration in the Japanese population.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 636, doi. 10.1007/s10038-007-0162-1
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- Article
Origins and genetic features of the Okhotsk people, revealed by ancient mitochondrial DNA analysis.
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- Journal of Human Genetics, 2007, v. 52, n. 7, p. 618, doi. 10.1007/s10038-007-0164-z
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- Article