Found: 30
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Breaking waves down under.
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- Nature Genetics, 1999, v. 22, n. 2, p. 117, doi. 10.1038/9617
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- Article
Chips for chimps.
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- Nature Genetics, 1999, v. 22, n. 2, p. 119, doi. 10.1038/9619
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Creating deaths from malaria.
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- Nature Genetics, 1999, v. 22, n. 2, p. 120, doi. 10.1038/9621
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You give me fever.
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- Nature Genetics, 1999, v. 22, n. 2, p. 121, doi. 10.1038/9624
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TOUCHINGbase.
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- Nature Genetics, 1999, v. 22, n. 2, p. 123
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- Article
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans.
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- Nature Genetics, 1999, v. 22, n. 2, p. 125, doi. 10.1038/9629
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Cloning of male mice from adult tail-tip cells.
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- Nature Genetics, 1999, v. 22, n. 2, p. 127, doi. 10.1038/9632
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Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.
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- Nature Genetics, 1999, v. 22, n. 2, p. 128, doi. 10.1038/9635
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An estimated frequency of endogenous insertional mutations in humans.
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- Nature Genetics, 1999, v. 22, n. 2, p. 130, doi. 10.1038/9638
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Imprinting and monogamy.
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- Nature Genetics, 1999, v. 22, n. 2, p. 130, doi. 10.1038/9639
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Genetic conflicts and the private life of Peromyscus polionotus.
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- Nature Genetics, 1999, v. 22, n. 2, p. 131, doi. 10.1038/9640
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The future of genetic counselling: an international perspective.
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- Nature Genetics, 1999, v. 22, n. 2, p. 133, doi. 10.1038/9641
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Prospects for whole-genome linkage disequilibrium mapping of common disease genes.
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- Nature Genetics, 1999, v. 22, n. 2, p. 139, doi. 10.1038/9642
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A polymorphism that affects OCT-1 binding to the TNF promoter region is associated with severe malaria.
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- Nature Genetics, 1999, v. 22, n. 2, p. 145, doi. 10.1038/9649
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Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.
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- Nature Genetics, 1999, v. 22, n. 2, p. 151, doi. 10.1038/9658
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The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein.
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- Nature Genetics, 1999, v. 22, n. 2, p. 159, doi. 10.1038/9667
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Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.
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- Nature Genetics, 1999, v. 22, n. 2, p. 164, doi. 10.1038/9674
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Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment.
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- Nature Genetics, 1999, v. 22, n. 2, p. 168, doi. 10.1038/9680
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A double-stranded RNA binding protein required for activation of repressed messages in mammalian germ cells.
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- Nature Genetics, 1999, v. 22, n. 2, p. 171, doi. 10.1038/9684
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Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome.
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- Nature Genetics, 1999, v. 22, n. 2, p. 175, doi. 10.1038/9691
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Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome.
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- Nature Genetics, 1999, v. 22, n. 2, p. 178, doi. 10.1038/9696
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The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase.
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- Nature Genetics, 1999, v. 22, n. 2, p. 182, doi. 10.1038/9700
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Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.
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- Nature Genetics, 1999, v. 22, n. 2, p. 188, doi. 10.1038/9707
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Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter.
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- Nature Genetics, 1999, v. 22, n. 2, p. 192, doi. 10.1038/9713
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Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
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- Nature Genetics, 1999, v. 22, n. 2, p. 196, doi. 10.1038/9718
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A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.
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- Nature Genetics, 1999, v. 22, n. 2, p. 199, doi. 10.1038/9722
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DNA methylation represses transcription in vivo.
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- Nature Genetics, 1999, v. 22, n. 2, p. 203, doi. 10.1038/9727
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Summer array.
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- Nature Genetics, 1999, v. 22, n. 2, p. 207, doi. 10.1038/9731
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Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.
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- Nature Genetics, 1999, v. 22, n. 2, p. 209, doi. 10.1038/9738
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Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome.
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- Nature Genetics, 1999, v. 22, n. 2, p. 209, doi. 10.1038/9735
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