{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,12]],"date-time":"2023-09-12T22:20:09Z","timestamp":1694557209285},"reference-count":13,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2013,5,25]],"date-time":"2013-05-25T00:00:00Z","timestamp":1369440000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Int Ophthalmol"],"published-print":{"date-parts":[[2014,4]]},"DOI":"10.1007\/s10792-013-9796-5","type":"journal-article","created":{"date-parts":[[2013,5,24]],"date-time":"2013-05-24T12:03:44Z","timestamp":1369397024000},"page":"351-354","source":"Crossref","is-referenced-by-count":5,"title":["Congenital glaucoma as an ophthalmic manifestation of Frank\u2013Ter Haar syndrome"],"prefix":"10.1007","volume":"34","author":[{"given":"Zeynep","family":"Aktas","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Emine Esra","family":"Karaca","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nurcan","family":"Dogan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tugba","family":"\u00c7akmak","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Metin","family":"Unlu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Levent","family":"Tok","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Murat","family":"Hasanreisoglu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2013,5,25]]},"reference":[{"key":"9796_CR1","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1002\/ajmg.a.30244","volume":"131","author":"SM Maas","year":"2004","unstructured":"Maas SM, Kayserili H, Lam J, Apak MY, Hennekam RCM (2004) Further delineation of Frank\u2013ter Haar syndrome. Am J Med Genet 131:127\u2013133","journal-title":"Am J Med Genet"},{"key":"9796_CR2","first-page":"67","volume":"21","author":"Y Frank","year":"1973","unstructured":"Frank Y, Ziprkowski M, Romano A, Stein R, Katznelson MB, Cohen B, Goodman RM (1973) Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome? J Genet Hum 21:67\u201372","journal-title":"J Genet Hum"},{"key":"9796_CR3","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1002\/ajmg.1320130418","volume":"13","author":"B Haar Ter","year":"1982","unstructured":"Ter Haar B, Hamel B, Hendriks J, de Jager J (1982) Melnick\u2013Needles syndrome: indication for an autosomal recessive form. Am J Med Genet 13:469\u2013477","journal-title":"Am J Med Genet"},{"key":"9796_CR4","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1002\/ajmg.1320560320","volume":"56","author":"BC Hamel","year":"1995","unstructured":"Hamel BC, Draaisma JMT, Pinckers AJ, Boetes C, Hoppe RL, Roppers HH, Brunner HG (1995) Autosomal recessive Melnick-Needles syndrome or Ter-Haar syndrome? report of a patient and reappraisal of an earlier report. Am J Med Genet 56:312\u2013316","journal-title":"Am J Med Genet"},{"key":"9796_CR5","doi-asserted-by":"crossref","first-page":"465","DOI":"10.1002\/ajmg.1320130417","volume":"13","author":"RJ Gorlin","year":"1982","unstructured":"Gorlin RJ, Knier J (1982) X-linked or autosomal dominant lethal in the male, inheritance of the Melnick-Needles (osteodysplasty) syndrome? a reappraisal. Am J Med Genet 13:465\u2013467","journal-title":"Am J Med Genet"},{"key":"9796_CR6","first-page":"2869","volume-title":"Nelson textbook of pediatrics","author":"WA Horton","year":"2007","unstructured":"Horton WA, Hecht JT (2007) The skeletal dysplasias. In: Behrman RE, Kliegman RM, Jenson HB (eds) Nelson textbook of pediatrics, 18th edn. Elsevier, Philadelphia, pp 2869\u20132887","edition":"18"},{"key":"9796_CR7","doi-asserted-by":"crossref","first-page":"1091","DOI":"10.1007\/s12098-011-0599-2","volume":"79","author":"P Femitha","year":"2012","unstructured":"Femitha P, Joy R, Gane BD, Adhisivam B, Bhat BV (2012) Frank\u2013Ter Haar Syndrome in a newborn. Indian J Pediatr 79:1091\u20131093","journal-title":"Indian J Pediatr"},{"key":"9796_CR8","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1002\/ajmg.a.30244","volume":"131","author":"SM Maas","year":"2004","unstructured":"Maas SM, Kayserili H, Lam J, Apak MY, Hennekam RC (2004) Further delineation of Frank\u2013ter Haar syndrome. Am J Med Genet 131:127\u2013133","journal-title":"Am J Med Genet"},{"key":"9796_CR9","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/j.ejmg.2009.03.005","volume":"52","author":"M Dundar","year":"2009","unstructured":"Dundar M, Saatci C, Tasdemir S, Akcakus M, Caglayan AO, Ozkul Y (2009) Frank\u2013ter Haar syndrome with unusual clinical features. Eur J Med Genet 52:247\u2013249","journal-title":"Eur J Med Genet"},{"key":"9796_CR10","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1002\/ajmg.1320130418","volume":"13","author":"B Haar Ter","year":"1982","unstructured":"Ter Haar B, Hamel B, Hendriks J, de Jager J (1982) Melnick\u2013Needles syndrome: indication for an autosomal recessive form. Am J Med Genet 13:469\u2013477","journal-title":"Am J Med Genet"},{"key":"9796_CR11","doi-asserted-by":"crossref","first-page":"e3","DOI":"10.1097\/IJG.0b013e318237cadf","volume":"22","author":"Z Aktas","year":"2013","unstructured":"Aktas Z, Yuksel N, Kula S, Akman A, Hasanreiso\u011flu B (2013) Childhood glaucoma as an ophthalmic manifestation of seckel syndrome. J Glaucoma 22:e3\u2013e4","journal-title":"J Glaucoma"},{"key":"9796_CR12","doi-asserted-by":"crossref","first-page":"165","DOI":"10.3109\/13816819209046485","volume":"13","author":"FD Verbraak","year":"1992","unstructured":"Verbraak FD, Pog\u00e1ny K, Pilon JW, Mooy CM, de France HF, Hennekam RC, Bleeker-Wagemakers EM (1992) Congennital glaucoma in a child with partial 1q duplicationa and 9p deletion. Ophthalmic Paediatr Genet 13:165\u2013170","journal-title":"Ophthalmic Paediatr Genet"},{"key":"9796_CR13","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1097\/01.mcd.0000077564.66911.0a","volume":"12","author":"A AlKaissi","year":"2003","unstructured":"AlKaissi A, Hammou A, Ghachem MB, Nacib MN, Chehida FB, Karoui H, Baraitser M (2003) Siblings with glaucoma, mental retardation and short stature. Clin Dysmorphol 12:191\u2013194","journal-title":"Clin Dysmorphol"}],"container-title":["International Ophthalmology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10792-013-9796-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10792-013-9796-5\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10792-013-9796-5","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,2,22]],"date-time":"2022-02-22T21:02:36Z","timestamp":1645563756000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10792-013-9796-5"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,5,25]]},"references-count":13,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2014,4]]}},"alternative-id":["9796"],"URL":"https:\/\/doi.org\/10.1007\/s10792-013-9796-5","relation":{},"ISSN":["0165-5701","1573-2630"],"issn-type":[{"value":"0165-5701","type":"print"},{"value":"1573-2630","type":"electronic"}],"subject":[],"published":{"date-parts":[[2013,5,25]]}}}