Found: 19
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The role of mutagenesis in defining genes in behaviour.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 651, doi. 10.1038/sj.ejhg.5201545
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- Article
The genetic basis of emotional behaviour in mice.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 721, doi. 10.1038/sj.ejhg.5201569
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- Article
Molecular genetics of the fruit-fly circadian clock.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 729, doi. 10.1038/sj.ejhg.5201547
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Genetics of affective (mood) disorders.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 660, doi. 10.1038/sj.ejhg.5201549
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- Article
Huntington's Disease: A transcriptional report card from the peripheral blood: Can it measure disease progression in Huntington's disease?
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 649, doi. 10.1038/sj.ejhg.5201562
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Molecular genetic studies of schizophrenia.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 669, doi. 10.1038/sj.ejhg.5201571
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- Article
The genetics of developmental dyslexia.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 681, doi. 10.1038/sj.ejhg.5201575
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Molecular analysis of a human PAX6 homeobox mutant.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 744, doi. 10.1038/sj.ejhg.5201579
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Genetics of intelligence.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 690, doi. 10.1038/sj.ejhg.5201588
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Genetics and pathophysiology of mental retardation.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 701, doi. 10.1038/sj.ejhg.5201595
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Focus on behavioural genetics.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 647, doi. 10.1038/sj.ejhg.5201599
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Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 752, doi. 10.1038/sj.ejhg.5201602
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Deletions of 2q14 that include the homeobox engrailed 1 (EN1) transcription factor are compatible with a normal phenotype.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 739, doi. 10.1038/sj.ejhg.5201605
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Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 768, doi. 10.1038/sj.ejhg.5201603
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SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 773, doi. 10.1038/sj.ejhg.5201611
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Genetics of autism spectrum disorder.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 714, doi. 10.1038/sj.ejhg.5201610
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Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 780, doi. 10.1038/sj.ejhg.5201612
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Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 759, doi. 10.1038/sj.ejhg.5201613
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Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity.
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- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 791, doi. 10.1038/sj.ejhg.5201614
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