{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,4]],"date-time":"2026-04-04T12:34:32Z","timestamp":1775306072142,"version":"3.50.1"},"reference-count":18,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2007,4]]},"DOI":"10.1097\/mcd.0b013e328054c404","type":"journal-article","created":{"date-parts":[[2007,3,6]],"date-time":"2007-03-06T08:52:56Z","timestamp":1173171176000},"page":"89-93","source":"Crossref","is-referenced-by-count":14,"title":["Warburg Micro syndrome in a Turkish boy"],"prefix":"10.1097","volume":"16","author":[{"given":"Adnan","family":"Y\u00fcksel","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G\u00f6zde","family":"Yesil","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cengiz","family":"Aras","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mehmet","family":"Seven","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-5-20211004","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1016\/S0161-6420(00)00540-6","article-title":"Micro syndrome in Muslim Pakistani children","volume":"108","author":"Ainsworth","year":"2001","journal-title":"Ophthalmology"},{"key":"R2-5-20211004","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1038\/ng1517","article-title":"Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome","volume":"37","author":"Aligianis","year":"2005","journal-title":"Nature Genet"},{"key":"R3-5-20211004","first-page":"343","article-title":"Syndrome of cataract, mild microcephaly, mental retardation and Perthes-like changes in sibs","volume":"30","author":"Czeizel","year":"1990","journal-title":"Acta Paediat Hung"},{"key":"R4-5-20211004","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1002\/ajmg.a.30109","article-title":"Congenital cataract, microphthalmia, hypoplasia of corpus callosum and hypogenitalism: report and review of micro syndrome","volume":"128A","author":"Derbent","year":"2004","journal-title":"Am J Med Genet"},{"key":"R5-5-20211004","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1086\/321295","article-title":"Cerebro-oculo- facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy","volume":"69","author":"Graham","year":"2001","journal-title":"Am J Hum Genet"},{"key":"R6-5-20211004","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1002\/ajmg.a.30060","article-title":"MICRO syndrome: an entity distinct from COFS syndrome","volume":"128A","author":"Graham","year":"2004","journal-title":"Am J Med Genet"},{"key":"R7-5-20211004","doi-asserted-by":"crossref","first-page":"397","DOI":"10.1136\/jmg.26.6.397","article-title":"Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndrome","volume":"26","author":"Harbord","year":"1989","journal-title":"J Med Genet"},{"key":"R8-5-20211004","first-page":"139","article-title":"A further example of a lethal autosomal recessive condition in sibs","volume":"16","author":"Laxova","year":"1972","journal-title":"J Ment Defic Res"},{"key":"R9-5-20211004","doi-asserted-by":"crossref","first-page":"282","DOI":"10.1016\/S0022-3476(71)80114-2","article-title":"Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: a new syndrome","volume":"79","author":"Lowry","year":"1971","journal-title":"J Pediat"},{"key":"R10-5-20211004","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1002\/ajmg.1320010305","article-title":"Severe mental retardation, cataracts, short stature and primary hypogonadism In two brothers","volume":"1","author":"Martsolf","year":"1978","journal-title":"Am J Med Genet"},{"key":"R11-5-20211004","first-page":"637","article-title":"Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?","volume":"36","author":"Megarbane","year":"1999","journal-title":"J Med Genet"},{"key":"R12-5-20211004","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1002\/ajmg.1320420115","article-title":"Cockayne syndrome: review of 140 cases","volume":"42","author":"Nance","year":"1992","journal-title":"Am J Med Genet"},{"key":"R13-5-20211004","doi-asserted-by":"crossref","first-page":"610","DOI":"10.1542\/peds.47.3.610","article-title":"A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings","volume":"47","author":"Neu","year":"1971","journal-title":"Pediatrics"},{"key":"R14-5-20211004","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1016\/S0022-3476(74)80119-8","article-title":"Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition","volume":"85","author":"Pena","year":"1974","journal-title":"J Pediat"},{"key":"R15-5-20211004","first-page":"241","article-title":"A second family with micro syndrome","volume":"8","author":"Rodriguez Criado","year":"1999","journal-title":"Clin Dysmorph"},{"key":"R16-5-20211004","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1001\/archpedi.1977.02120150049010","article-title":"A syndrome of microcephaly and cataracts in four siblings: a new genetic syndrome?","volume":"131","author":"Scott-Emuakpor","year":"1977","journal-title":"Am J Dis Child"},{"key":"R17-5-20211004","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1016\/S0022-3476(73)80198-2","article-title":"Syndrome of microcephaly, cataracts, kyphosis, and joint contractures versus Cockayne syndrome","volume":"82","author":"Sugarman","year":"1973","journal-title":"J Pediat"},{"key":"R19-5-20211004","doi-asserted-by":"crossref","first-page":"1309","DOI":"10.1001\/archpedi.1993.02160360051017","article-title":"Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism: micro syndrome","volume":"147","author":"Warburg","year":"1993","journal-title":"Am J Dis Child"}],"container-title":["Clinical Dysmorphology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/00019605-200704000-00005","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,10]],"date-time":"2023-05-10T21:40:14Z","timestamp":1683754814000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00019605-200704000-00005"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,4]]},"references-count":18,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2007]]}},"URL":"https:\/\/doi.org\/10.1097\/mcd.0b013e328054c404","relation":{},"ISSN":["0962-8827"],"issn-type":[{"value":"0962-8827","type":"print"}],"subject":[],"published":{"date-parts":[[2007,4]]}}}