Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
about
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).Hematopoietic Stem Cell Transplantation in an Infant with Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome.Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation.Regulation of the Development and Function of B Cells by ZBTB Transcription Factors.
P2860
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
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
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
@en
type
label
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
@en
prefLabel
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
@en
P2093
P2860
P50
P1476
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
@en
P2093
Alain Fischer
Delphine Sterlin
Felipe Suarez
Guillaume Velasco
P2860
P2888
P304
P356
10.1007/S10875-016-0240-2
P577
2016-02-06T00:00:00Z
P6179
1048115089