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<italic>ZNF687</italic> mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 6, p. 1240, doi. 10.1111/cge.13247
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- Publication type:
- Article
Autosomal‐dominant myopia associated to a novel <italic>P4HA2</italic> missense variant and defective collagen hydroxylation.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 5, p. 982, doi. 10.1111/cge.13217
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- Publication type:
- Article
A functional allelic variant of the FGF23 gene is associated with renal phosphate leak in calcium nephrolithiasis.
- Published in:
- 2012
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- Publication type:
- Journal Article
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort.
- Published in:
- Neurogenetics, 2012, v. 13, n. 1, p. 97, doi. 10.1007/s10048-011-0312-7
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- Publication type:
- Article
Hospitalisation risks in the treatment of schizophrenia in a Medicaid population: comparison of antipsychotic medications.
- Published in:
- International Journal of Clinical Practice, 2006, v. 60, n. 11, p. 1419, doi. 10.1111/j.1742-1241.2006.01161.x
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- Publication type:
- Article
The evolutionary conservation of the human chitotriosidase gene in rodents and primates.
- Published in:
- Cytogenetic & Genome Research, 2004, v. 105, n. 1, p. 54, doi. 10.1159/000078009
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- Publication type:
- Article
Methods for Claims-Based Pharmacoeconomic Studies in Psychosis.
- Published in:
- PharmacoEconomics, 2002, v. 20, n. 8, p. 499, doi. 10.2165/00019053-200220080-00001
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- Publication type:
- Article
Use of healthcare services by patients treated with risperidone versus conventional antipsychotic agents.
- Published in:
- 2002
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- Publication type:
- journal article
Characterization of the murine orthologue of a novel human subtelomeric multigene family.
- Published in:
- Cytogenetics & Cell Genetics, 2001, v. 94, n. 1/2, p. 98, doi. 10.1159/000048796
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- Publication type:
- Article
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene.
- Published in:
- Cytogenetics & Cell Genetics, 1999, v. 84, n. 3/4, p. 164, doi. 10.1159/000015247
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- Publication type:
- Article