Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH.
about
Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant.Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome).A Whole Germline BRCA2 Gene Deletion: How to Learn from CNV In Silico Analysis.
P2860
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH.
description
2017 nî lūn-bûn
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name
Diagnostic application of a ca ...... nd copy number as well as LOH.
@en
Diagnostic application of a ca ...... nd copy number as well as LOH.
@nl
type
label
Diagnostic application of a ca ...... nd copy number as well as LOH.
@en
Diagnostic application of a ca ...... nd copy number as well as LOH.
@nl
prefLabel
Diagnostic application of a ca ...... nd copy number as well as LOH.
@en
Diagnostic application of a ca ...... nd copy number as well as LOH.
@nl
P2093
P2860
P50
P356
P1433
P1476
Diagnostic application of a ca ...... and copy number as well as LOH
@en
P2093
E Manolakos
I Limongelli
P2860
P304
P356
10.1111/CGE.13060
P577
2017-09-15T00:00:00Z