Found: 12
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A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 12, p. 3137, doi. 10.1002/ajmg.a.35664
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- Article
Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0052239
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- Article
C21orf91 Genotypes Correlate With Herpes Simplex Labialis (Cold Sore) Frequency: Description of a Cold Sore Susceptibility Gene.
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- Journal of Infectious Diseases, 2011, v. 204, n. 11, p. 1654, doi. 10.1093/infdis/jir633
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- Article
Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia.
- Published in:
- Birth Defects Research, 2018, v. 110, n. 7, p. 610, doi. 10.1002/bdr2.1223
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- Article
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.
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- Molecular Autism, 2014, v. 5, n. 1, p. 3, doi. 10.1186/2040-2392-5-5
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- Article
Carriers of Rare Missense Variants in IFIH1 Are Protected from Psoriasis.
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- Journal of Investigative Dermatology, 2010, v. 130, n. 12, p. 2768, doi. 10.1038/jid.2010.214
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- Article
Further Genetic Evidence for Three Psoriasis-Risk Genes: ADAM33, CDKAL1, and PTPN22.
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- Journal of Investigative Dermatology, 2009, v. 129, n. 3, p. 629, doi. 10.1038/jid.2008.297
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- Article
Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0160653
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- Article
A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 7, p. 1, doi. 10.1371/journal.pgen.1000125
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- Article
The 5q31 variants associated with psoriasis and Crohn's disease are distinct.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 19, p. 2978, doi. 10.1093/hmg/ddn196
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- Article
Evidence for Linkage on Chromosome 3q25–27 in a Large Autism Extended Pedigree.
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- Human Heredity, 2005, v. 60, n. 4, p. 220, doi. 10.1159/000090546
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- Article
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes.
- Published in:
- Nicotine & Tobacco Research, 2009, v. 11, n. 7, p. 785, doi. 10.1093/ntr/ntp064
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- Article