Suchergebnisse - "Attwood, Antony"

1

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

von: Westbury, Sarah K

2015, in: Genome medicine

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2

Transcriptional diversity during lineage commitment of human blood progenitors

von: Chen, Lu

2014, in: Science

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3

Genetic studies of body mass index yield new insights for obesity biology

von: Locke, Adam E

2015, in: Nature

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4

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

von: Tuijnenburg, Paul

2018, in: Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward

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5

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

von: Burton, Paul R.

2007, in: Nature

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6

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

von: Burton, Paul R

2007, in: Nature genetics

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7

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

von: Nejentsev, Sergey

2007, in: Nature

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