Epigenetic modifications in cancer.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 303, doi. 10.1111/j.1399-0004.2011.01809.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2012 AND VI 81 AND IP 4
Results: 14
1
2
Lysosomal multienzymatic complex-related diseases: a genetic study among Portuguese patients.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 379, doi. 10.1111/j.1399-0004.2011.01625.x
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- Publication type:
- Article
3
Schizophrenia as variation in the sapiens-specific epigenetic instruction to the embryo.
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- Clinical Genetics, 2012, v. 81, n. 4, p. 319, doi. 10.1111/j.1399-0004.2012.01830.x
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- Publication type:
- Article
4
Integrating genomic and epigenomic information: a promising strategy for identifying functional DNA variants of human disease.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 334, doi. 10.1111/j.1399-0004.2011.01840.x
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- Publication type:
- Article
5
Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 350, doi. 10.1111/j.1399-0004.2011.01822.x
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- Publication type:
- Article
6
Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/ H19 in Silver-Russell syndrome.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 366, doi. 10.1111/j.1399-0004.2012.01844.x
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- Publication type:
- Article
7
It is ALL about the 6p22 histone gene cluster: characterizing the unique genetic features of Down's syndrome patients.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 364, doi. 10.1111/j.1399-0004.2011.01837.x
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- Publication type:
- Article
8
The early-life social environment and DNA methylation.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 341, doi. 10.1111/j.1399-0004.2012.01843.x
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- Publication type:
- Article
9
Association of genomic deletions in the STXBP1 gene with Ohtahara syndrome.
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- Clinical Genetics, 2012, v. 81, n. 4, p. 399, doi. 10.1111/j.1399-0004.2011.01733.x
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- Publication type:
- Article
10
Getting to the bottom of autism spectrum and related disorders: MBD5 as a key contributor.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 363, doi. 10.1111/j.1399-0004.2011.01836.x
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- Publication type:
- Article
11
What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 325, doi. 10.1111/j.1399-0004.2011.01795.x
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- Publication type:
- Article
12
Epigenetics of colorectal cancer.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 312, doi. 10.1111/j.1399-0004.2011.01829.x
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- Publication type:
- Article
13
BAG3-related myofibrillar myopathy in a Chinese family.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 394, doi. 10.1111/j.1399-0004.2011.01659.x
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- Publication type:
- Article
14
A new era of non-invasive prenatal genetic diagnosis: exploiting fetal epigenetic differences.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 4, p. 362, doi. 10.1111/j.1399-0004.2011.01835.x
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- Publication type:
- Article