{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,5]],"date-time":"2026-03-05T21:13:51Z","timestamp":1772745231799,"version":"3.50.1"},"reference-count":16,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[1996,4,1]],"date-time":"1996-04-01T00:00:00Z","timestamp":828316800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1996,4]]},"DOI":"10.1007\/bf02267083","type":"journal-article","created":{"date-parts":[[2005,12,8]],"date-time":"2005-12-08T17:20:24Z","timestamp":1134062424000},"page":"540-542","source":"Crossref","is-referenced-by-count":2,"title":["Congenital alacrima in a patient with G (Opitz Frias) syndrome"],"prefix":"10.1007","volume":"97","author":[{"given":"Munis","family":"Dundar","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kuddusi","family":"Erkili\u00e7","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fatma","family":"Demiryilmaz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mustafa","family":"K\u00fc\u00e7\u00fckaydin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mustafa","family":"Kendirci","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hamit","family":"Okur","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ahmet","family":"Kazez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02267083_CR1","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1002\/ajmg.1320280207","volume":"28","author":"M Cappa","year":"1987","unstructured":"Cappa M, Borrelli P, Marini R, Neri G (1987) The Opitz syndrome: a new designation for the clinically indistinguishable BBB and G syndromes. Am J Med Genet 28:303\u2013310","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR2","doi-asserted-by":"crossref","first-page":"422","DOI":"10.1002\/ajmg.1320370324","volume":"37","author":"J Christodoulou","year":"1990","unstructured":"Christodoulou J, Bankier A, Loughnan P (1990) Ring chromosome 22 karyotype in a patient with Opitz (BBBG) syndrome (letter). Am J Med Genet 37:422\u2013424","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR3","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1002\/ajmg.1320020205","volume":"2","author":"JF Cordero","year":"1978","unstructured":"Cordero JF, Holmes LB (1978) Phenotypic overlap of the BBB and G syndrome. Am J Med Genet 2:145\u2013152","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR4","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1111\/j.1399-0004.1981.tb02066.x","volume":"19","author":"GB Cote","year":"1981","unstructured":"Cote GB, Katsantoni A, Papadakou-Lagoyanni S, Costalos C, Timotheou T, Skordalakis A, Deligerorgis D, Pantelakis S (1981) The G syndrome of dysphagia, ocular hypertelorism and hypospadias. Clin Genet 19:473\u2013478","journal-title":"Clin Genet"},{"key":"BF02267083_CR5","first-page":"913","volume-title":"System of ophthalmology, vol 3, part 2","author":"SS Duke-Elder","year":"1963","unstructured":"Duke-Elder SS (1963) Congenital deformities. In: Duke-Elder SS (ed) System of ophthalmology, vol 3, part 2. Kimpton, London, pp 913\u2013916"},{"key":"BF02267083_CR6","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1002\/ajmg.1320260319","volume":"26","author":"E Ehrich","year":"1987","unstructured":"Ehrich E, Aranoff G, Johnson WG (1987) Familial achalasia associated with adrenocortical insufficiency, alacrima, and neurological abnormalities. Am J Med Genet 26:637\u2013644","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR7","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1002\/ajmg.1320020204","volume":"2","author":"SJ Funderburk","year":"1978","unstructured":"Funderburk SJ, Stewart R (1978) The G and BBB syndromes: case presentations, genetics and nosology. Am J Med Genet 2:131\u2013144","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR8","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1002\/ajmg.1320030111","volume":"3","author":"CR Greenberg","year":"1979","unstructured":"Greenberg CR, Schraufnagel D (1979) The g syndrome: a case report. Am J Med Genet 3:59\u201364","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR9","doi-asserted-by":"crossref","first-page":"800","DOI":"10.1016\/0002-9394(86)90416-2","volume":"102","author":"GC Keith","year":"1986","unstructured":"Keith GC, Boldt DW (1986) Congenital absence of the lacrimal gland. Am J Ophthalmol 102:800\u2013801","journal-title":"Am J Ophthalmol"},{"key":"BF02267083_CR10","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1002\/ajmg.1320400210","volume":"40","author":"LG Leichtman","year":"1991","unstructured":"Leichtman LG, Werner A, Bass WT, Smith D, Brothman AR (1991) Apparent Opitz BBBG syndrome with a partial duplication of 5p. Am J Med Genet 40:173\u2013176","journal-title":"Am J Med Genet"},{"key":"BF02267083_CR11","first-page":"505","volume":"121","author":"JR Little","year":"1971","unstructured":"Little JR, Opitz JM (1971) The G syndrome. Am J Dis Child 121:505\u2013507","journal-title":"Am J Dis Child"},{"key":"BF02267083_CR12","first-page":"51","volume-title":"Mendelian inheritance in man","author":"VA McKusick","year":"1994","unstructured":"McKusick VA (1994) Mendelian inheritance in man, 9th edn. Johns Hopkins University Press, Baltimore London, pp 51, 759","edition":"9th edn."},{"key":"BF02267083_CR13","first-page":"86","volume-title":"The clinical delineation of birth defects. II. Malformation syndromes, vol 5, part 2","author":"JM Opitz","year":"1969","unstructured":"Opitz JM, Summitt RL, Smith DW (1969a) The BBB syndrome. Familial telecanthus with associated congenital abnormalies. In: Bergsma D (ed) The clinical delineation of birth defects. II. Malformation syndromes, vol 5, part 2. The National Foundation-March of Dimes, New York, pp 86\u201394"},{"key":"BF02267083_CR14","first-page":"95","volume-title":"The clinical delineation of birth defects. II. Malformation syndromes, vol 5, part 2","author":"JM Opitz","year":"1969","unstructured":"Opitz JM, Frias JL, Gutenberg JE, Pellet JR (1969b) The G syndrome of multiple congenital anomalies. In: Bergsma D (ed) The clinical delineation of birth defects. II. Malformation syndromes, vol 5, part 2. The National Foundation-March of Dimes, New York, pp 95\u2013101"},{"key":"BF02267083_CR15","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1542\/peds.3.4.468","volume":"3","author":"CM Riley","year":"1949","unstructured":"Riley CM, Day RL, Greeley D, Langford WS (1949) Central autonomic dysfunction with defective lacrimation. 1. Report of five cases. Pediatrics 3:468","journal-title":"Pediatrics"},{"key":"BF02267083_CR16","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1002\/ajmg.1320340303","volume":"34","author":"A Verloes","year":"1989","unstructured":"Verloes A, Le Mener M, Briard M-L (1989) BBBG syndrome or Opitz syndrome: new family. Am J Med Genet 34:313\u2013316","journal-title":"Am J Med Genet"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02267083.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02267083\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02267083","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,5]],"date-time":"2023-05-05T20:39:12Z","timestamp":1683319152000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02267083"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,4]]},"references-count":16,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1996,4]]}},"alternative-id":["BF02267083"],"URL":"https:\/\/doi.org\/10.1007\/bf02267083","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,4]]}}}