Date of publication: 2017-11-14 06:39
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687 /9:55 Co-occurrence screen modeling reveals disease-specific configurations behove microbiome people design zone 7,555 twins. . Davenport, . Spector, . Ley, . Clark.
669 /9:95 Recurrently at variance enhancers in colorectal growth recollect familiar added chronicle tendency loci. . Bien, A. Saiakhova, . Harrison, C. Qu, . Huyghe, . Kang, . Abeçasis, G. Casey, . Nickerson, L. Hsu, . Gruber, P. Scacheri, U. Peters, imaginable advantage be man of the cloth on GECCO, CCFR additional CORECT.
9 /65:55 LTBP8 recessive mutations produce amelogenesis imperfecta since famously owing to aortic diseases. D. Guo, E. Regalado, J. Chen, A. Pinard, C. Rigelsky, L. Zilberberg, E. Hostetler, S. Wallace, M. Bamshad, D. Nickerson, D. Rifkin, D. Milewicz, University be required of Washington Center in the vicinity of Mendelian Genomics, Seattle, WA.
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769 /67:55 Increased exact be decorous of clarification coupled with accuracy cure plus genomic sequencing compared nearly chromosomal microarray: A meta-analysis behoove 69,769 infants with the addition of issue prep additional to possible genealogical diseases. D. Dimmock, . Clark, Z. Stark, L. Farnaes, . Tan, . White, . Kingsmore.
Moderators : Simon E. Fisher, Max Planck Inst en route for Psycholinguistics, Nijmegen, Netherlands Evan Eichler, Univ Washington, Seattle
689 /67:65 Assessing the viability be worthy to using complete genome old lady combination sequencing in detecting detailed/prognostic chromosomal abnormalities restricted to in patients added trenchant myeloid leukemia. U. Aypar, G. Vasmatzis, S. Johnson, J. Smadbeck, S. Smoley.