Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
about
Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency and autism.Clinical exome sequencing in France and Quebec: what are the challenges? What does the future hold?Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases
P2860
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
description
2017 nî lūn-bûn
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2017年学术文章
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name
Using medical exome sequencing ...... inical units and 216 patients.
@en
Using medical exome sequencing ...... inical units and 216 patients.
@nl
type
label
Using medical exome sequencing ...... inical units and 216 patients.
@en
Using medical exome sequencing ...... inical units and 216 patients.
@nl
prefLabel
Using medical exome sequencing ...... inical units and 216 patients.
@en
Using medical exome sequencing ...... inical units and 216 patients.
@nl
P2093
P2860
P50
P356
P1433
P1476
Using medical exome sequencing ...... linical units and 216 patients
@en
P2093
A Jacquette
C Depienne
P2860
P304
P356
10.1111/CGE.13102
P577
2017-10-04T00:00:00Z