Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability.
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Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Application of whole-exome seq ...... with intellectual disability.
@en
Application of whole-exome seq ...... with intellectual disability.
@nl
type
label
Application of whole-exome seq ...... with intellectual disability.
@en
Application of whole-exome seq ...... with intellectual disability.
@nl
prefLabel
Application of whole-exome seq ...... with intellectual disability.
@en
Application of whole-exome seq ...... with intellectual disability.
@nl
P2093
P2860
P356
P1476
Application of whole-exome seq ...... with intellectual disability.
@en
P2093
Alexandra Gauthier-Vasserot
Ange-Line Bruel
Christel Thauvin-Robinet
Claire Briandet
Daniel Amram
Daphné Lehalle
Delphine Heron
Elodie Gautier
Frédéric Huet
Isabelle Maystadt
P2860
P356
10.1002/AJMG.A.37969
P407
P577
2016-09-12T00:00:00Z