A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome.
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New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome.Toward health technology assessment of whole-genome sequencing diagnostic tests: challenges and solutions
P2860
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A maternal deletion upstream o ...... l Beckwith-Wiedemann syndrome.
@en
type
label
A maternal deletion upstream o ...... l Beckwith-Wiedemann syndrome.
@en
prefLabel
A maternal deletion upstream o ...... l Beckwith-Wiedemann syndrome.
@en
P2093
P2860
P356
P1476
A maternal deletion upstream o ...... l Beckwith-Wiedemann syndrome.
@en
P2093
Bernhard Horsthemke
Hermann-Josef Lüdecke
Ivana Joksic
Jasmin Beygo
Julia Kolarova
Karin Buiting
Tim M Strom
Zeljko Mikovic
P2860
P2888
P304
P356
10.1038/EJHG.2016.3
P577
2016-02-03T00:00:00Z
P6179
1022373866