Found: 11
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Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
- Published in:
- Nature, 1994, v. 371, n. 6494, p. 252, doi. 10.1038/371252a0
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- Article
Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry.
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- Obesity Facts: The European Journal of Obesity, 2011, v. 4, n. 2, p. 131, doi. 10.1159/000327797
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- Article
TFAP2B Influences the Effect of Dietary Fat on Weight Loss under Energy Restriction.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043212
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- Article
Dietary Factors Impact on the Association between CTSS Variants and Obesity Related Traits.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040394
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- Article
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038663
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- Article
Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 3, p. 353, doi. 10.1038/ejhg.2010.180
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- Article
Technical Validation of a Reverse-Transcription Quantitative Polymerase Chain Reaction In Vitro Diagnostic Test for the Determination of MiR-31-3p Expression Levels in Formalin-Fixed Paraffin-Embedded Metastatic Colorectal Cancer Tumor Specimens.
- Published in:
- Biomarker Insights, 2018, n. 13, p. 1, doi. 10.1177/1177271918763357
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- Article
Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.
- Published in:
- BMC Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2156-10-16
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- Publication type:
- Article
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 16, p. 2541, doi. 10.1093/hmg/ddn154
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- Article
Association of autism with polymorphisms in the paired-likehomeodomain transcription factor 1 (PITX1) on chromosome 5q31:a candidate gene analysis.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 74, doi. 10.1186/1471-2350-8-74
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- Publication type:
- Article
Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 11, doi. 10.1186/1471-2350-8-11
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- Publication type:
- Article