Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.
about
22q11 deletion syndrome: current perspective.Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implicationsCanadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: outflow tract obstruction, coarctation of the aorta, tetralogy of Fallot, Ebstein anomaly and Marfan's syndromeRare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathwaysPrevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.Clinically detectable copy number variations in a Canadian catchment population of schizophrenia.Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot.Premature death in adults with 22q11.2 deletion syndrome.Response to clozapine in a clinically identifiable subtype of schizophrenia.Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature reviewPerceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome.Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome.Functional outcomes of adults with 22q11.2 deletion syndrome1q21.1 Microduplication expression in adults.Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.Changing lesion demographics of the adult with congenital heart disease: an emerging population with complex needs.Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients.
P2860
Q27687449-7704ADF6-6E52-42CA-9CD4-32D074A2DF06Q28298135-07A17031-CD48-4EE3-B081-9CA2CE4731EDQ33776426-630B7FA5-09BC-489B-B0D9-A26FBF81AA22Q34388498-2C77F9CC-4101-4C2E-9D73-A0B6CADF07DFQ34507393-2629E516-638B-4049-A002-EB7C9B102DEBQ35085481-40148B0B-D8A4-4FB3-BF44-E866E91DE3C9Q35124137-E1950D2B-C281-412C-A5D7-8128732BC265Q35281099-3B5A7D04-F4DB-4A87-9DBC-E4E4FE7B2E2EQ35695451-201684DA-CCB2-4FD3-A616-77F2F6D82ED2Q35695460-099F1180-CF80-4C2D-9ECA-E93065C9A8AEQ35731550-82030ED4-227C-4940-944F-495DB5C7A4C4Q35809316-062382EF-6943-4DF2-9B01-3A6AFF05DD9AQ35893090-53F5C5B1-47E2-4D2E-9CEB-EE26110BC881Q36052504-8149048F-5933-45E7-97FB-CAF93CD5B079Q36301370-4AF45D22-BFF0-408B-892F-04E5AE384760Q37278755-9B067DA6-0C2A-42F0-A72D-CC4DAAC44CA5Q37470598-C3C7D6FC-3529-4475-B2E2-34D22E56A02CQ37993153-01F968FB-8431-4427-912B-02CD65091294Q38542088-D1E56ADD-9EAC-4452-B40D-B39220CF0024Q47136130-C665C503-790D-4B42-9B45-07E20F54F66A
P2860
Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Extracardiac features predicti ...... dult congenital heart disease.
@ast
Extracardiac features predicti ...... dult congenital heart disease.
@en
type
label
Extracardiac features predicti ...... dult congenital heart disease.
@ast
Extracardiac features predicti ...... dult congenital heart disease.
@en
prefLabel
Extracardiac features predicti ...... dult congenital heart disease.
@ast
Extracardiac features predicti ...... dult congenital heart disease.
@en
P2093
P2860
P1476
Extracardiac features predicti ...... dult congenital heart disease.
@en
P2093
Anne S Bassett
Eva W C Chow
Gary D Webb
Michael A Gatzoulis
Wai Lun Alan Fung
P2860
P356
10.1016/J.IJCARD.2007.08.141
P577
2008-01-11T00:00:00Z