{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,9]],"date-time":"2025-09-09T20:59:33Z","timestamp":1757451573023},"reference-count":23,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2012,12]]},"DOI":"10.1097\/anc.0b013e318276c320","type":"journal-article","created":{"date-parts":[[2012,11,27]],"date-time":"2012-11-27T10:39:56Z","timestamp":1354012796000},"page":"336-342","source":"Crossref","is-referenced-by-count":7,"title":["CHARGE Syndrome"],"prefix":"10.1097","volume":"12","author":[{"given":"Tracey","family":"Allen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"issue":"2","key":"R1-5-20210316","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1016\/S0022-3476(81)80454-4","article-title":"Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association.","volume":"99","author":"Pagon","year":"1981","journal-title":"J Pediatr"},{"issue":"9","key":"R4-5-20210316","doi-asserted-by":"crossref","first-page":"995","DOI":"10.1038\/ng1407","article-title":"Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.","volume":"36","author":"Vissers","year":"2004","journal-title":"Nature Genet"},{"key":"R7-5-20210316","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1038\/sj.ejhg.5201778","article-title":"CHARGE syndrome: an update.","volume":"15","author":"Sanlaville","year":"2007","journal-title":"Eur J Hum Genet"},{"key":"R8-5-20210316","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1136\/jmg.2005.036061","article-title":"CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.","volume":"43","author":"Jongmans","year":"2006","journal-title":"J Med Genet"},{"key":"R10-5-20210316","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1038\/sj.ejhg.5201778","article-title":"CHARGE syndrome: an update.","volume":"15","author":"Sanlaville","year":"2007","journal-title":"Eur J Hum Genet"},{"key":"R11-5-20210316","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1002\/ajmg.a.30559","article-title":"Updated diagnostic criteria for CHARGE syndrome: a proposal.","volume":"133A","author":"Verloes","year":"2005","journal-title":"Am J Med Genet"},{"key":"R12-5-20210316","doi-asserted-by":"crossref","first-page":"410","DOI":"10.1016\/j.jpeds.2005.10.044","article-title":"Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.","volume":"118","author":"Aramaki","year":"2006","journal-title":"J Pediatr"},{"key":"R13-5-20210316","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1111\/j.1399-0004.2008.01014.x","article-title":"CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome.","volume":"74","author":"Wincent","year":"2008","journal-title":"Clin Genet"},{"key":"R14-5-20210316","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1002\/ajmg.a.30560","article-title":"An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study.","volume":"133A","author":"Issekutz","year":"2005","journal-title":"Am J Med Genet"},{"key":"R15-5-20210316","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1086\/500273","article-title":"Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.","volume":"78","author":"Lalani","year":"2006","journal-title":"Am J Hum Genet"},{"key":"R16-5-20210316","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1111\/j.1399-0004.1996.tb02736.x","article-title":"Increased paternal age in CHARGE association.","volume":"50","author":"Tellier","year":"1996","journal-title":"Clin Genet"},{"issue":"3","key":"R17-5-20210316","doi-asserted-by":"crossref","first-page":"395","DOI":"10.1016\/S0022-3476(79)80513-2","article-title":"Choanal atresia and associated multiple anomalies.","volume":"95","author":"Hall","year":"1979","journal-title":"J Pediatr"},{"key":"R18-5-20210316","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1177\/000992289803700302","article-title":"CHARGE association: an update and review for the primary pediatrician.","volume":"37","author":"Blake","year":"1998","journal-title":"Clin Pediatr"},{"key":"R19-5-20210316","first-page":"2093","article-title":"Whats your diagnosis: simple iris coloboma.","volume":"40","author":"Schneiderman","year":"2000","journal-title":"Consultant"},{"issue":"3","key":"R20-5-20210316","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1016\/S0039-6257(00)00151-X","article-title":"Ocular colobomata.","volume":"45","author":"Onwochei","year":"2000","journal-title":"Surv Opthalmol"},{"issue":"10","key":"R21-5-20210316","doi-asserted-by":"crossref","first-page":"5621","DOI":"10.1210\/jc.2004-2474","article-title":"CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development.","volume":"90","author":"Pinto","year":"2005","journal-title":"J Clin Endocrinol Metabol"},{"key":"R22-5-20210316","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1007\/s00455-004-0026-1","article-title":"Early oral sensory experiences and feeding development in children with CHARGE syndrome: a report of five cases.","volume":"20","author":"Dobbelsteyn","year":"2005","journal-title":"Dysphagia"},{"key":"R23-5-20210316","doi-asserted-by":"crossref","first-page":"228","DOI":"10.1002\/1096-8628(20000918)94:3<228::AID-AJMG8>3.0.CO;2-H","article-title":"Hypogonadism and CHARGE association.","volume":"94","author":"Wheeler","year":"2000","journal-title":"Am J Med Genet"},{"issue":"6","key":"R24-5-20210316","doi-asserted-by":"crossref","first-page":"e1594","DOI":"10.1542\/peds.2010-0164","article-title":"Delayed puberty due to a novel mutation in CHD7 causing CHARGE syndrome.","volume":"126","author":"Dauber","year":"2010","journal-title":"Pediatrics"},{"key":"R25-5-20210316","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1111\/j.1399-0004.2008.01107.x","article-title":"CHD7 mutations in patients initially diagnoses with Kallmann syndromethe clinical overlap with CHARGE syndrome.","volume":"75","author":"Jongmans","year":"2009","journal-title":"Clin Gen"},{"key":"R26-5-20210316","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1002\/1096-8628(20010301)99:2<124::AID-AJMG1114>3.0.CO;2-9","article-title":"Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome.","volume":"99","author":"Amiel","year":"2001","journal-title":"Am J Med Genet"},{"key":"R27-5-20210316","doi-asserted-by":"crossref","first-page":"e871","DOI":"10.1542\/peds.2008-3400","article-title":"CHARGE syndrome and chromosome 22q11.2 Deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features.","volume":"123","author":"Jyonouchi","year":"2009","journal-title":"Pediatrics"},{"issue":"1","key":"R28-5-20210316","doi-asserted-by":"crossref","first-page":"43","DOI":"10.3121\/cmr.1.1.43","article-title":"Immune deficiency in CHARGE association.","volume":"1","author":"Theodoropoulos","year":"2003","journal-title":"Clin Med Res"}],"container-title":["Advances in Neonatal Care"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/journals.lww.com\/00149525-201212000-00005","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,4,10]],"date-time":"2021-04-10T05:28:02Z","timestamp":1618032482000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00149525-201212000-00005"}},"subtitle":["Diagnosis and Clinical Management in the NICU"],"short-title":[],"issued":{"date-parts":[[2012,12]]},"references-count":23,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2012]]}},"URL":"https:\/\/doi.org\/10.1097\/anc.0b013e318276c320","relation":{},"ISSN":["1536-0903"],"issn-type":[{"value":"1536-0903","type":"print"}],"subject":[],"published":{"date-parts":[[2012,12]]}}}