About: Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

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article by Ashleigh A Richards et al published October 2008 in Pediatric Research

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2008 (fr) наукова стаття, опублікована в жовтні 2008 (uk) im Oktober 2008 veröffentlichter wissenschaftlicher Artikel (de) article by Ashleigh A Richards et al published October 2008 in Pediatric Research (en)
publication date	wds:Q57828177-CDBE8C7B-5C1B-4B2B-9084-70E788405A01
publication date	2008-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57828177-2032B0B8-85A5-4270-B5FE-33ECB68A2BD4
language of work or name	English
exact match	wds:Q57828177-60D527E7-7CFC-408B-BACC-D44AE39D632F
exact match	https://scigraph.springernature.com/pub.10.1203/pdr.0b013e31818095d0
cites work	wds:Q57828177-093B88E6-22D0-4496-AFAF-711533ECDE38 wds:Q57828177-1398949E-BDC6-4C93-A9B5-F12444DCCBA7 wds:Q57828177-5253EC44-931C-4614-852A-809791FC64A2 wds:Q57828177-5997CC2A-650D-4154-8BAC-0DFAAA24397D wds:Q57828177-5F786F32-9E4E-4C5D-8E07-43D774DC0D38 wds:Q57828177-5FA15A6F-D48E-466E-BCB0-E527BD1ED66D wds:Q57828177-619BAA3E-A63F-4789-A6AC-E0BD405EC4A6 wds:Q57828177-6338EB03-7BA1-4EA2-9B24-6E5DB144AD80 wds:Q57828177-78418117-6DE6-4CC0-B917-EFE3E96BC159 wds:Q57828177-7B7E1EF5-17B9-44AD-9151-1E859B817225 wds:Q57828177-871C9CE5-7D4C-49CB-B41E-A208CCAC77C7 wds:Q57828177-91686602-E0D4-4430-8EE2-305148FB5048 wds:Q57828177-94F3897C-8F0A-4B17-814A-42A594736D4D wds:Q57828177-A8181C02-1DF1-4CF2-9583-0BD0A6EE520E wds:Q57828177-AA617C9E-27D4-463D-A5C2-46EAED549057 wds:Q57828177-AF471E06-F980-4EA0-BF22-5EE6D49E403B wds:Q57828177-D576E0AA-4DBD-49B7-9D51-9F25420008FF wds:Q57828177-D57F458C-1816-4C2A-A148-AF6117E58F0D wds:Q57828177-E61CEDC5-EE20-416E-9AE6-DCC87078D1E9 wds:Q57828177-E7787DBE-D63D-4B49-800F-6B5FCE53C6AF wds:Q57828177-F2EFB107-641B-45DC-9661-4586AFC603FD wds:Q57828177-F5CB6057-4D64-4FD3-988B-6FFD9F9A7B8F wds:Q57828177-F7D172D7-6229-48B9-BB6F-FB703AF1CB7C wds:Q57828177-FC13AC01-2E11-446C-B3CB-D9A9F6250FC3
cites work	Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors The incidence of congenital heart disease A faster circular binary segmentation algorithm for the analysis of array CGH data Insights into the genetic basis of congenital heart disease. Strong association of de novo copy number mutations with autism Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients Identification of disease genes by whole genome CGH arrays Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports Causes of congenital heart diseases: old and new modes, mechanisms, and models Human cytogenetics: 46 chromosomes, 46 years and counting. The genetics of cardiac birth defects Copy number variations and clinical cytogenetic diagnosis of constitutional disorders Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Copy number variation in the human genome and its implications for cardiovascular disease Genetic basis of congenital heart disease DiGeorge syndrome: the use of model organisms to dissect complex genetics Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group Kousseff syndrome: a causally heterogeneous disorder. The genetic contribution to congenital heart disease Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).
author name string	wds:Q57828177-0B3942D6-C78D-4C12-AC62-CF2CF774DC0C wds:Q57828177-4878878D-6587-4C63-AEB3-C332EAE3E871 wds:Q57828177-64AE40DD-8DAB-4938-BF35-FF5FB89F1013 wds:Q57828177-6BF059D5-919B-46B4-9A3B-112446775FD5 wds:Q57828177-7D55ACBF-98BA-4250-8CD3-CFCC643B2B66 wds:Q57828177-7E327774-4133-4D83-AA72-AE1F94EC5838
author name string	Natalie S Hauser Frederick F Elder Haley A Nichols Ashleigh A Richards Bill P Crider Lane Jaeckle Santos
rdfs:label	Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (en) Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (nl)
skos:prefLabel	Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (en) Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (nl)
name	Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (en) Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (nl)
author	wds:Q57828177-858FC967-B5D7-4C25-91A6-7D66E08BBA73 wds:Q57828177-F00846DA-0C58-45B5-A4F3-0F5775CE5DAB
author	Vidu Garg Andrew R. Zinn
title	wds:Q57828177-BE8C0F36-C35A-40B8-A1CC-2919406B3853
title	Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (en)
page(s)	wds:Q57828177-73C1BA14-507E-4F93-BDF7-605B9D9D71B5
page(s)	358-363
instance of	wds:Q57828177-E6E6C924-5B9C-4BFD-8C07-399E66CF46F7
instance of	scholarly article
main subject	wds:Q57828177-EA2253D6-7645-43E9-B8E1-F413F6E15985
main subject	congenital heart disease
PubMed ID	wds:Q57828177-49D651B1-8A1C-47C6-9F85-B4CCC7B5EC6E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18535492
PubMed ID	18535492
published in	wds:Q57828177-20F582AB-8BB6-4A82-82EB-973FD1E6F778
published in	Pediatric Research
issue	wds:Q57828177-B69E4D25-0F9A-4784-87F6-AD5FAFCA2FAE
volume	wds:Q57828177-0B7642EA-D35B-407F-9D72-75DA88B05DEC
issue	4
volume	64
DOI	wds:Q57828177-CBB99828-43D9-4D95-A134-681D0A0A36FE

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