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A POTENTIAL GENOMIC BIOMARKER FOR THE DETECTION OF POLYCYCLIC AROMATIC HYDROCARBON POLLUTANTS: MULTIDRUG RESISTANCE GENE 49 IN DROSOPHILA MELANOGASTER.
- Published in:
- Environmental Toxicology & Chemistry, 2007, v. 26, n. 7, p. 1418, doi. 10.1897/06-552R.1
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- Publication type:
- Article
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
- Published in:
- 2019
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- Publication type:
- journal article
Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 11, p. 1072, doi. 10.1002/pd.2613
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- Publication type:
- Article
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report.
- Published in:
- Genes, 2024, v. 15, n. 2, p. 225, doi. 10.3390/genes15020225
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- Publication type:
- Article
Longest form of CCTG microsatellite repeat in the promoter of the CD2BP1/PSTPIP1 gene is associated with aseptic abscesses and with Crohn disease in French patients.
- Published in:
- 2010
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- Publication type:
- journal article
Detection of trisomy 21 by quantitative fluorescentpolymerase chain reaction in uncultured amniocytes.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 4, p. 287, doi. 10.1002/pd.579
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- Publication type:
- Article
Leucoencephalopathy with vanishing white matter may cause progressive myoclonus epilepsy.
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- Epilepsia (Series 4), 2008, v. 49, n. 5, p. 910, doi. 10.1111/j.1528-1167.2008.01542.x
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- Publication type:
- Article
Subcommissural organ/Reissner's fiber complex: Characterization of SCO-spondin, a glycoprotein with potent activity on neurite outgrowth.
- Published in:
- Glia, 2000, v. 32, n. 2, p. 177, doi. 10.1002/1098-1136(200011)32:2<177::AID-GLIA70>3.0.CO;2-V
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- Publication type:
- Article
Pathological Implications of Receptor for Advanced Glycation End-Product (AGER) Gene Polymorphism.
- Published in:
- Disease Markers, 2019, p. 1, doi. 10.1155/2019/2067353
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- Publication type:
- Article
Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.
- Published in:
- 2009
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- Publication type:
- Other
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
- Published in:
- Human Mutation, 2000, v. 16, n. 2, p. 143, doi. 10.1002/1098-1004(200008)16:2<143::AID-HUMU7>3.0.CO;2-J
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- Publication type:
- Article
A phase-II study based on dose adjustment according to UGT1A1 polymorphism: is irinotecan underdosed in first-line FOLFIRI regimen for mCRC?
- Published in:
- Cancer Chemotherapy & Pharmacology, 2024, v. 93, n. 3, p. 225, doi. 10.1007/s00280-023-04603-x
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- Publication type:
- Article
Insertion of mutant proteolipid protein results in missorting of myelin proteins (This article is a US Government work and, as such, is in the public domain in the United States of America.).
- Published in:
- Annals of Neurology, 2003, v. 54, n. 6, p. 769
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- Publication type:
- Article