Works matching IS 1756994X AND DT 2014 AND VI 6 AND IP 5
Results: 4
Copy number variants are a common cause of non-syndromic hearing loss.
- Published in:
- Genome Medicine, 2014, v. 6, n. 5, p. 1, doi. 10.1186/gm554
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- Publication type:
- Article
Gene expression profiles associated with acute myocardial infarction and risk of cardiovascular death.
- Published in:
- Genome Medicine, 2014, v. 6, n. 5, p. 64, doi. 10.1186/gm560
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- Publication type:
- Article
Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin.
- Published in:
- Genome Medicine, 2014, v. 6, n. 5, p. 42, doi. 10.1186/gm559
- By:
- Publication type:
- Article
Returning individual research results for genome sequences of pancreatic cancer.
- Published in:
- Genome Medicine, 2014, v. 6, n. 5, p. 22, doi. 10.1186/gm558
- By:
- Publication type:
- Article