Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosis.
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Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosis.
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
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-hant
name
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@en
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@nl
type
label
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@en
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@nl
prefLabel
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@en
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@nl
P2093
P1476
Concurrent occurrence of an in ...... ures, and lambdoid synostosis.
@en
P2093
Hiroshi Tokimura
Hisashi Tsuru
Kazunori Arita
Keiko Shimojima
Mayumi Matsufuji
Nayuta Higa
Nozomi Sano
Tatsuki Oyoshi
Yumiko Ondo
P304
P356
10.1016/J.EJMG.2016.10.006
P577
2016-10-14T00:00:00Z