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Editorial
. 2016 Jan 29;8(1):12.
doi: 10.1186/s13073-016-0265-4.

From genomic medicine to precision medicine: highlights of 2015

Affiliations
Editorial

From genomic medicine to precision medicine: highlights of 2015

Charles Auffray et al. Genome Med. .
No abstract available

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References

    1. Deciphering Developmental Disorders Study Large-scale discovery of novel genetic causes of developmental disorders. Nature. 2015;519:223–228. - PMC - PubMed
    1. Akawi N, McRae J, Ansari M, Balasubramanian M, Blyth M, Brady AF, et al. Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. Nat Genet. 2015;47:1363–1369. doi: 10.1038/ng.3410. - DOI - PMC - PubMed
    1. Chong JX, Buckingham KJ, Jhangiani SN, Boehm C, Sobreira N, Smith JD, et al. The genetic basis of Mendelian phenotypes: discoveries, challenges, and opportunities. Am J Hum Genet. 2015;97:199–215. doi: 10.1016/j.ajhg.2015.06.009. - DOI - PMC - PubMed
    1. Miller NA, Farrow EG, Gibson M, Willig LK, Twist G, Yoo B, et al. A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases. Genome Med. 2015;7:100. doi: 10.1186/s13073-015-0221-8. - DOI - PMC - PubMed
    1. Smedley D, Robinson PN. Phenotype-driven strategies for exome prioritization of human Mendelian disease genes. Genome Med. 2015;7:81. doi: 10.1186/s13073-015-0199-2. - DOI - PMC - PubMed

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