2012 highlights in translational 'omics.

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The emergence of top-down proteomics in clinical research Defining tissue proteomes by systematic literature review.

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2012 highlights in translational 'omics.

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2013 nî lūn-bûn

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2013年論文

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2013年論文

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2013年论文

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2012 highlights in translational 'omics.

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2012 highlights in translational 'omics.

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2012 highlights in translational 'omics.

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2012 highlights in translational 'omics.

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James R Lupski

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Matthias Schwab

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Timothy Veenstra

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P2860

Estimating the human mutation rate using autozygosity in a founder population

Rate of de novo mutations and the importance of father's age to disease risk

Public health action in genomics is now needed beyond newborn screening

Cystic fibrosis in an era of genomically guided therapy

Mapping intact protein isoforms in discovery mode using top-down proteomics

Quantifying your body: a how-to guide from a systems biology perspective

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Personal omics profiling reveals dynamic molecular and medical phenotypes

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.

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gm414

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Timothy Caulfield

Charles Auffray

Muin J. Khoury

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2013-01-31T00:00:00Z

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2012 highlights in translational 'omics.

about

P2860

P2860

2012 highlights in translational 'omics.

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