Isolated hypermethylation of GRB10 (7p12.2) in a Silver-Russell syndrome patient carrying a 20p13 microdeletion.
about
New developments in Silver-Russell syndrome and implications for clinical practiceEMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome.Multilocus methylation defects in imprinting disorders.Structural and sequence variants in patients with Silver-Russell syndrome or similar features-Curation of a disease database.
P2860
Isolated hypermethylation of GRB10 (7p12.2) in a Silver-Russell syndrome patient carrying a 20p13 microdeletion.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Isolated hypermethylation of G ...... arrying a 20p13 microdeletion.
@en
Isolated hypermethylation of GRB10
@nl
type
label
Isolated hypermethylation of G ...... arrying a 20p13 microdeletion.
@en
Isolated hypermethylation of GRB10
@nl
prefLabel
Isolated hypermethylation of G ...... arrying a 20p13 microdeletion.
@en
Isolated hypermethylation of GRB10
@nl
P2093
P2860
P356
P1433
P1476
Isolated hypermethylation of G ...... arrying a 20p13 microdeletion.
@en
P2093
B Schneider-Rätzke
M Begemann
S Spengler
T Eggermann
P2860
P304
P356
10.1111/CGE.12186
P577
2013-06-10T00:00:00Z