Novel treatment strategies for schizophrenia from improved understanding of genetic risk.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 401, doi. 10.1111/cge.12485
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2014 AND VI 86 AND IP 5
Results: 18
1
2
Use of genetic technologies to compare medicines.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 441, doi. 10.1111/cge.12462
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- Publication type:
- Article
3
From the era of genome analysis to the era of genomic drug discovery: a pioneering example of rheumatoid arthritis.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 432, doi. 10.1111/cge.12465
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- Publication type:
- Article
4
Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 469, doi. 10.1111/cge.12414
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- Publication type:
- Article
5
'When atlastin meets spastin'.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 504, doi. 10.1111/cge.12331
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- Publication type:
- Article
6
Translational genomics and head and neck cancer: toward precision medicine.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 412, doi. 10.1111/cge.12487
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- Publication type:
- Article
7
Autosomal dominant IFIH1 gain-of-function mutations cause Aicardi-Goutières syndrome.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 473, doi. 10.1111/cge.12471
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- Publication type:
- Article
8
Role of the Nrf2 signaling system in health and disease.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 447, doi. 10.1111/cge.12474
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- Publication type:
- Article
9
De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 492, doi. 10.1111/cge.12300
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- Publication type:
- Article
10
Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 482, doi. 10.1111/cge.12304
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- Publication type:
- Article
11
Molecular and phenotypic characterization of atypical Williams-Beuren syndrome.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 487, doi. 10.1111/cge.12305
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- Publication type:
- Article
12
Genetic regulation of vertebrate eye development.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 453, doi. 10.1111/cge.12493
- By:
- Publication type:
- Article
13
Whole exome analysis identifies dominant COL4A1 mutations in patients with complex ocular phenotypes involving microphthalmia.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 475, doi. 10.1111/cge.12379
- By:
- Publication type:
- Article
14
Views of primary care providers regarding the return of genome sequencing incidental findings.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 461, doi. 10.1111/cge.12390
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- Publication type:
- Article
15
Charcot-Marie-Tooth disease and pathways to molecular based therapies.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 422, doi. 10.1111/cge.12393
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- Publication type:
- Article
16
Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 500, doi. 10.1111/cge.12312
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- Publication type:
- Article
17
Preventing ovarian cancer through genetic testing: a population-based study.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 496, doi. 10.1111/cge.12313
- By:
- Publication type:
- Article
18
Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 5, p. 502, doi. 10.1111/cge.12319
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- Publication type:
- Article