Works matching IS 03406717 AND DT 2010 AND VI 128 AND IP 3
Results: 11
Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 325, doi. 10.1007/s00439-010-0854-z
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- Publication type:
- Article
Genome-wide association identifies a deletion in the 3′ untranslated region of Striatin in a canine model of arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 315, doi. 10.1007/s00439-010-0855-y
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- Publication type:
- Article
Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 233, doi. 10.1007/s00439-010-0852-1
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- Publication type:
- Article
Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 303, doi. 10.1007/s00439-010-0856-x
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- Publication type:
- Article
Association between colony-stimulating factor 1 receptor gene polymorphisms and asthma risk.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 293, doi. 10.1007/s00439-010-0850-3
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- Publication type:
- Article
Regional differences in awareness and attitudes regarding genetic testing for disease risk and ancestry.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 249, doi. 10.1007/s00439-010-0845-0
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- Publication type:
- Article
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.
- Published in:
- 2010
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- Publication type:
- Report
CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 281, doi. 10.1007/s00439-010-0848-x
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- Publication type:
- Article
An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental Jews.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 261, doi. 10.1007/s00439-010-0846-z
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- Publication type:
- Article
Genome-wide searching of rare genetic variants in WTCCC data.
- Published in:
- Human Genetics, 2010, v. 128, n. 3, p. 269, doi. 10.1007/s00439-010-0849-9
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- Publication type:
- Article
Bonnie S. LeRoy, Patricia McCarthy Veach, Dianne M. Bartels (eds): Genetic counselling practice: advanced concepts and skills.
- Published in:
- 2010
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- Publication type:
- Book Review