Found: 10
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Integrating common and rare genetic variation in diverse human populations.
- Published in:
- Nature, 2010, v. 467, n. 7311, p. 52, doi. 10.1038/nature09298
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- Publication type:
- Article
Somatic mutations affect key pathways in lung adenocarcinoma.
- Published in:
- Nature, 2008, v. 455, n. 7216, p. 1069, doi. 10.1038/nature07423
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- Publication type:
- Article
The DNA sequence, annotation and analysis of human chromosome 3.
- Published in:
- 2006
- By:
- Publication type:
- Letter
The finished DNA sequence of human chromosome 12.
- Published in:
- Nature, 2006, v. 440, n. 7082, p. 346, doi. 10.1038/nature04569
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- Publication type:
- Article
Suptavumab for the Prevention of Medically Attended Respiratory Syncytial Virus Infection in Preterm Infants.
- Published in:
- Clinical Infectious Diseases, 2021, v. 73, n. 11, p. e4400, doi. 10.1093/cid/ciaa951
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- Publication type:
- Article
Genome sequence of the Brown Norway rat yields insights into mammalian evolution.
- Published in:
- Nature, 2004, v. 428, n. 6982, p. 493, doi. 10.1038/nature02426
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- Publication type:
- Article
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 17, p. 3366, doi. 10.1093/hmg/ddr243
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- Publication type:
- Article
Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 4, p. 1, doi. 10.1371/journal.pgen.1003443
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- Publication type:
- Article
Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing.
- Published in:
- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 18, p. 1869, doi. 10.1001/jama.2014.14601
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- Publication type:
- Article
Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy.
- Published in:
- Genome Medicine, 2013, v. 5, n. 6, p. 1, doi. 10.1186/gm461
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- Publication type:
- Article