Found: 15
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Expression and localization of CHODL<sub>ΔE</sub>/CHODL<sub>fΔE</sub>, the soluble isoform of chondrolectin
- Published in:
- Cell Biology International, 2007, v. 31, n. 11, p. 1323, doi. 10.1016/j.cellbi.2007.05.014
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- Article
Expression profile of telomerase subunits in human pleural mesothelioma.
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- Journal of Pathology, 2000, v. 190, n. 1, p. 80, doi. 10.1002/(SICI)1096-9896(200001)190:1<80::AID-PATH498>3.0.CO;2-7
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- Article
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
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- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1090, doi. 10.1038/sj.ejhg.5201674
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- Article
Molecular and clinical examination of an Italian DEFECT 11 family.
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- European Journal of Human Genetics, 1999, v. 7, n. 5, p. 579, doi. 10.1038/sj.ejhg.5200339
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- Article
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.
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- Brain: A Journal of Neurology, 2006, v. 129, n. 11, p. 2977, doi. 10.1093/brain/awl203
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- Article
Biotechnology in the capital region of Europe.
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- Journal of Commercial Biotechnology, 2010, v. 16, n. 2, p. 168, doi. 10.1057/jcb.2009.34
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- Article
Differentiation-Dependent Alternative Splicing and Expression of the Extracellular Matrix Protein 1 Gene in Human Keratinocytes.
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- Journal of Investigative Dermatology, 2000, v. 114, n. 4, p. 718, doi. 10.1046/j.1523-1747.2000.00916.x
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- Article
Europe is speeding up R&D in deep submicron processing.
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- Solid State Technology, 1998, v. 41, n. 6, p. 50
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- Article
Fully automated FISH examination of amniotic fluid cells.
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- Prenatal Diagnosis, 2007, v. 27, n. 10, p. 951, doi. 10.1002/pd.1806
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- Article
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
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- Human Mutation, 2006, v. 27, n. 9, p. 914, doi. 10.1002/humu.20350
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- Article
Nonsyndromic hearing impairment is associated with a mutation in DFNA5.
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- Nature Genetics, 1998, v. 20, n. 2, p. 194, doi. 10.1038/2503
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- Article
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) (Communicated by Ulf Landegren).
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- Human Mutation, 2004, v. 23, n. 1, p. 17, doi. 10.1002/humu.10300
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- Article
Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses.
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- Human Molecular Genetics, 1996, v. 5, n. 10, p. 1547, doi. 10.1093/hmg/5.10.1547
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- Article
X-linked liver glycogenosis: localization and isolation of a candidate gene.
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- Human Molecular Genetics, 1993, v. 2, n. 5, p. 583
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- Article
Frequency of the phenylalanine deletion (ΔF.
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- Clinical Genetics, 1991, v. 39, n. 2, p. 89, doi. 10.1111/j.1399-0004.1991.tb02992.x
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- Article