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'Early Neolithic' graves of the Carpathian Basin are in fact 6000 years younger-Appeal for real interdisciplinarity between archaeology and ancient DNA research.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 467, doi. 10.1038/jhg.2012.36
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Detection of a large heterozygous deletion and a splicing defect in the CFTR transcripts from nasal swab of a Japanese case of cystic fibrosis.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 427, doi. 10.1038/jhg.2012.46
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Response to Data on Hungarian Early Neolithic graves by Bánffy et al.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 470, doi. 10.1038/jhg.2012.64
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- Article
High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 442, doi. 10.1038/jhg.2012.49
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Haplotype analysis of ESR2 in Japanese patients with spermatogenic failure.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 449, doi. 10.1038/jhg.2012.53
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- Article
Association of variants in genes involved in environmental chemical metabolism and risk of cryptorchidism and hypospadias.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 434, doi. 10.1038/jhg.2012.48
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- Article
An abundance of population-specific monomorphic SNPs may or may not be meaningful: a commentary on differences in allele frequencies of familial hypercholesterolemia SNPs in the Malaysian population.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 403, doi. 10.1038/jhg.2012.52
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- Article
Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 422, doi. 10.1038/jhg.2012.45
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A Commentary on Association of variants in genes involved in environmental chemical metabolism and risk of cryptorchidism and hypospadias.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 405, doi. 10.1038/jhg.2012.76
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- Article
Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 453, doi. 10.1038/jhg.2012.56
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- Article
Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 459, doi. 10.1038/jhg.2012.57
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- Article
A cautionary note on the reporting of genetic association study results.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 465, doi. 10.1038/jhg.2012.47
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- Article
Danon disease: focusing on heart.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 407, doi. 10.1038/jhg.2012.72
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- Article
Comprehensive evaluation of imputation performance in African Americans.
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- Journal of Human Genetics, 2012, v. 57, n. 7, p. 411, doi. 10.1038/jhg.2012.43
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- Article