Utility of next generation sequencing in clinical primary immunodeficiencies.
about
Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn.Exome and genome sequencing for inborn errors of immunity.Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from Turkey.Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.Next-generation sequencing for identifying genetic mutations in adults with bronchiectasis.The United Kingdom Primary Immune Deficiency (UKPID) registry 2012 to 2017
P2860
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P2860
Utility of next generation sequencing in clinical primary immunodeficiencies.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Utility of next generation sequencing in clinical primary immunodeficiencies.
@ast
Utility of next generation sequencing in clinical primary immunodeficiencies.
@en
type
label
Utility of next generation sequencing in clinical primary immunodeficiencies.
@ast
Utility of next generation sequencing in clinical primary immunodeficiencies.
@en
prefLabel
Utility of next generation sequencing in clinical primary immunodeficiencies.
@ast
Utility of next generation sequencing in clinical primary immunodeficiencies.
@en
P2093
P2860
P1476
Utility of next generation sequencing in clinical primary immunodeficiencies.
@en
P2093
Christina E Ciaccio
Darrell L Dinwiddie
Douglas Swanson
Nikita Raje
Sarah Soden
P2860
P2888
P356
10.1007/S11882-014-0468-Y
P577
2014-10-01T00:00:00Z