Works matching IS 03406717 AND DT 2016 AND VI 135 AND IP 6
Results: 8
A Clinician's perspective on clinical exome sequencing.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 643, doi. 10.1007/s00439-016-1662-x
- By:
- Publication type:
- Article
Discovery of mutations for Mendelian disorders.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 615, doi. 10.1007/s00439-016-1664-8
- By:
- Publication type:
- Article
Deciphering intratumor heterogeneity using cancer genome analysis.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 635, doi. 10.1007/s00439-016-1670-x
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- Publication type:
- Article
Regulating whole exome sequencing as a diagnostic test.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 655, doi. 10.1007/s00439-016-1677-3
- By:
- Publication type:
- Article
Discovery of rare variants for complex phenotypes.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 625, doi. 10.1007/s00439-016-1679-1
- By:
- Publication type:
- Article
The journey of exome sequencing from disease mutations discovery to clinical genomics.
- Published in:
- 2016
- By:
- Publication type:
- Editorial
Clinical genomics: from a truly personal genome viewpoint.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 591, doi. 10.1007/s00439-016-1682-6
- By:
- Publication type:
- Article
Novel bioinformatic developments for exome sequencing.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 603, doi. 10.1007/s00439-016-1658-6
- By:
- Publication type:
- Article