{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T21:31:41Z","timestamp":1768512701339,"version":"3.49.0"},"reference-count":33,"publisher":"Oxford University Press (OUP)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,3]]},"DOI":"10.1093\/eurheartj\/ehq447","type":"journal-article","created":{"date-parts":[[2010,12,19]],"date-time":"2010-12-19T01:32:52Z","timestamp":1292722372000},"page":"568-573","source":"Crossref","is-referenced-by-count":10,"title":["Familial ventricular aneurysms and septal defects map to chromosome 10p15"],"prefix":"10.1093","volume":"32","author":[{"given":"Nicolas","family":"Tremblay","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shi Wei","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marc-Phillip","family":"Hitz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G\u00e9raldine","family":"Asselin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jonathan","family":"Ginns","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kathleen","family":"Riopel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roxanne","family":"Gendron","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexandre","family":"Montpetit","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Edwina","family":"Duhig","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marie-Pierre","family":"Dub\u00e9","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dorothy","family":"Radford","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gregor","family":"Andelfinger","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2010,12,18]]},"reference":[{"key":"key\n\t\t\t\t20170515123406_EHQ447C1","doi-asserted-by":"crossref","first-page":"472","DOI":"10.1111\/j.1651-2227.2008.01152.x","article-title":"Congenital heart disease in 111 225 births in Belgium: birth prevalence, treatment and survival in the 21st century","volume":"98","year":"2009","journal-title":"Acta Paediatr"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C2","doi-asserted-by":"crossref","first-page":"516","DOI":"10.1111\/j.1399-0004.2008.01009.x","article-title":"Genetic factors in congenital heart malformation","volume":"73","year":"2008","journal-title":"Clin Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C3","doi-asserted-by":"crossref","first-page":"2179","DOI":"10.1093\/eurheartj\/ehi378","article-title":"Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect","volume":"26","year":"2005","journal-title":"Eur Heart J"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C4","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1038\/ng1526","article-title":"Mutation in myosin heavy chain 6 causes atrial septal defect","volume":"37","year":"2005","journal-title":"Nat Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C5","doi-asserted-by":"crossref","first-page":"1650","DOI":"10.1016\/j.jacc.2003.05.004","article-title":"NKX2.5 mutations in patients with congenital heart disease","volume":"42","year":"2003","journal-title":"J Am Coll Cardiol"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C6","first-page":"1953","article-title":"Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects","volume":"16","year":"2007","journal-title":"Eur Heart J"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C7","first-page":"779","article-title":"GATA4 sequence variants in patients with congenital heart disease","volume":"4","year":"2007","journal-title":"J Med Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C8","first-page":"91","article-title":"Genetic epidemiology of congenital heart diseases","volume":"5","year":"1983","journal-title":"Prog Med Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C9","first-page":"111","article-title":"Familial recurrence of congenital heart disease: an overview and review of the literature","volume":"166","year":"2007","journal-title":"Eur J Pediatr"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C10","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1017\/S1047951107000996","article-title":"Familial muscular ventricular septal defects and aneurysms of the muscular interventricular septum","volume":"17","year":"2007","journal-title":"Cardiol Young"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C11","doi-asserted-by":"crossref","first-page":"742","DOI":"10.1093\/bioinformatics\/17.8.742","article-title":"GRR: graphical representation of relationship errors","volume":"17","year":"2001","journal-title":"Bioinformatics"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C12","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1086\/301904","article-title":"PedCheck: a program for identification of genotype incompatibilities in linkage analysis","volume":"63","year":"1998","journal-title":"Am J Hum Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C13","doi-asserted-by":"crossref","first-page":"2123","DOI":"10.1093\/bioinformatics\/bti264","article-title":"ALOHOMORA: a tool for linkage analysis using 10K SNP array data","volume":"21","year":"2005","journal-title":"Bioinformatics"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C14","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1038\/ng786","article-title":"Merlin\u2014rapid analysis of dense genetic maps using sparse gene flow trees","volume":"30","year":"2002","journal-title":"Nat Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C15","doi-asserted-by":"crossref","first-page":"3565","DOI":"10.1093\/bioinformatics\/bti571","article-title":"easyLINKAGE-Plus\u2014automated linkage analyses using large-scale SNP data","volume":"21","year":"2005","journal-title":"Bioinformatics"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C16","first-page":"1347","article-title":"Parametric and nonparametric linkage analysis: a unified multipoint approach","volume":"58","year":"1996","journal-title":"Am J Hum Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C17","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1038\/ng1416","article-title":"Detection of large-scale variation in the human genome","volume":"36","year":"2004","journal-title":"Nat Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C18","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1007\/s00246-001-0007-1","article-title":"Autosomal dominant myocardial disease diagnosed by fetal presentation of proband with an aneurysm of the muscular interventricular septum","volume":"23","year":"2002","journal-title":"Pediatr Cardiol"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C19","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1007\/s002460010246","article-title":"Congenital aneurysm of the muscular interventricular septum in a fraternal case diagnosed by fetal echocardiography","volume":"22","year":"2001","journal-title":"Pediatr Cardiol"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C20","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1007\/s002469900297","article-title":"Familial occurrence of congenital aneurysm of the muscular interventricular septum","volume":"19","year":"1998","journal-title":"Pediatr Cardiol"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C21","doi-asserted-by":"crossref","first-page":"104","DOI":"10.1136\/hrt.65.2.104","article-title":"Familial aneurysms of the interventricular septum","volume":"65","year":"1991","journal-title":"Br Heart J"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C22","first-page":"47","article-title":"Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect","volume":"135","year":"2005","journal-title":"Am J Med Genet A"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C23","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1038\/ng917","article-title":"A high-resolution recombination map of the human genome","volume":"31","year":"2002","journal-title":"Nat Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C24","doi-asserted-by":"crossref","first-page":"7548","DOI":"10.1073\/pnas.112212199","article-title":"Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly","volume":"99","year":"2002","journal-title":"Proc Natl Acad Sci USA"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C25","doi-asserted-by":"crossref","first-page":"e1000522","DOI":"10.1371\/journal.pgen.1000522","article-title":"Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening","volume":"5","year":"2009","journal-title":"PLoS Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C26","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1086\/426833","article-title":"Long-range control of gene expression: emerging mechanisms and disruption in disease","volume":"76","year":"2005","journal-title":"Am J Hum Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C27","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1038\/ng.329","article-title":"Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence","volume":"41","year":"2009","journal-title":"Nat Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C28","doi-asserted-by":"crossref","first-page":"1357","DOI":"10.1182\/blood-2005-05-1916","article-title":"Developmental regulation of yolk sac hematopoiesis by Kruppel-like factor 6","volume":"107","year":"2006","journal-title":"Blood"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C29","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1007\/s00109-002-0331-9","article-title":"Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p","volume":"80","year":"2002","journal-title":"J Mol Med"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C30","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1038\/sj.ejhg.5200183","article-title":"Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)","volume":"6","year":"1998","journal-title":"Eur J Hum Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C31","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1111\/j.1399-0004.2004.00290.x","article-title":"Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome","volume":"66","year":"2004","journal-title":"Clin Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C32","doi-asserted-by":"crossref","first-page":"524","DOI":"10.1016\/j.ajhg.2009.03.010","article-title":"DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources","volume":"84","year":"2009","journal-title":"Am J Hum Genet"},{"key":"key\n\t\t\t\t20170515123406_EHQ447C33","doi-asserted-by":"crossref","first-page":"931","DOI":"10.1038\/ng.415","article-title":"De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot","volume":"41","year":"2009","journal-title":"Nat Genet"}],"container-title":["European Heart Journal"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/eurheartj\/article-pdf\/32\/5\/568\/17049670\/ehq447.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,6,7]],"date-time":"2019-06-07T05:48:28Z","timestamp":1559886508000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/eurheartj\/article-lookup\/doi\/10.1093\/eurheartj\/ehq447"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,12,18]]},"references-count":33,"journal-issue":{"issue":"5","published-online":{"date-parts":[[2010,12,18]]},"published-print":{"date-parts":[[2011,3]]}},"URL":"https:\/\/doi.org\/10.1093\/eurheartj\/ehq447","relation":{},"ISSN":["0195-668X","1522-9645"],"issn-type":[{"value":"0195-668X","type":"print"},{"value":"1522-9645","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010,12,18]]}}}