Found: 14
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Mitochondrial DNA and inflammatory diseases.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 161, doi. 10.1007/s00439-011-1057-y
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- Publication type:
- Article
A novel transcript of cyclin-dependent kinase-like 5 ( CDKL5) has an alternative C-terminus and is the predominant transcript in brain.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 187, doi. 10.1007/s00439-011-1058-x
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- Publication type:
- Article
Preimplantation genetic diagnosis: State of the ART 2011.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 175, doi. 10.1007/s00439-011-1056-z
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- Publication type:
- Article
Mitochondrial Haplogroup X is associated with successful aging in the Amish.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 201, doi. 10.1007/s00439-011-1060-3
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- Publication type:
- Article
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 209, doi. 10.1007/s00439-011-1062-1
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- Publication type:
- Article
Meta-analysis of new genome-wide association studies of colorectal cancer risk.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 217, doi. 10.1007/s00439-011-1055-0
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- Publication type:
- Article
The cell adhesion gene PVRL3 is associated with congenital ocular defects.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 235, doi. 10.1007/s00439-011-1064-z
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- Publication type:
- Article
The impact of Converso Jews on the genomes of modern Latin Americans.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 251, doi. 10.1007/s00439-011-1072-z
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- Publication type:
- Article
Successful COG8 and PDF overlap is mediated by alterations in splicing and polyadenylation signals.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 265, doi. 10.1007/s00439-011-1075-9
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- Publication type:
- Article
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 289, doi. 10.1007/s00439-011-1076-8
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- Publication type:
- Article
Analysis of family- and population-based samples in cohort genome-wide association studies.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 275, doi. 10.1007/s00439-011-1071-0
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- Publication type:
- Article
Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 301, doi. 10.1007/s00439-011-1078-6
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- Publication type:
- Article
Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q.
- Published in:
- Human Genetics, 2012, v. 131, n. 2, p. 311, doi. 10.1007/s00439-011-1134-2
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- Publication type:
- Article
Michelle Webb (ed): Cancer Susceptibility: Methods and Protocols.
- Published in:
- 2012
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- Publication type:
- Book Review