about
The importance of copy number variation in congenital heart diseaseDe Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual Disabilities.Identification of CASZ1 NES reveals potential mechanisms for loss of CASZ1 tumor suppressor activity in neuroblastoma.Detection of 1p36 deletion by clinical exome-first diagnostic approach.The Growing Complexity of the Monosomy 1p36 SyndromePhenotype of a Patient With a 1p36.11-p35.3 Interstitial Deletion Encompassing the AHDC1Genotype-phenotype correlations in individuals with pathogenic RERE variants.Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.SRARP and HSPB7 are epigenetically regulated gene pairs that function as tumor suppressors and predict clinical outcome in malignancies.Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015 թուականին հրատարակուած գիտական յօդուած
@hyw
2015 թվականին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
name
1p36 deletion syndrome: an update
@ast
1p36 deletion syndrome: an update
@en
1p36 deletion syndrome: an update
@nl
type
label
1p36 deletion syndrome: an update
@ast
1p36 deletion syndrome: an update
@en
1p36 deletion syndrome: an update
@nl
prefLabel
1p36 deletion syndrome: an update
@ast
1p36 deletion syndrome: an update
@en
1p36 deletion syndrome: an update
@nl
P2093
P2860
P3181
P356
P1476
1p36 deletion syndrome: an update
@en
P2093
Daryl A Scott
Hitisha P Zaveri
Valerie K Jordan
P2860
P304
P3181
P356
10.2147/TACG.S65698
P407
P577
2015-01-01T00:00:00Z