{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,16]],"date-time":"2026-05-16T03:03:34Z","timestamp":1778900614563,"version":"3.51.4"},"reference-count":60,"publisher":"Springer Science and Business Media LLC","issue":"5","license":[{"start":{"date-parts":[[1996,5,1]],"date-time":"1996-05-01T00:00:00Z","timestamp":830908800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Pediatr"],"published-print":{"date-parts":[[1996,5]]},"DOI":"10.1007\/bf01955267","type":"journal-article","created":{"date-parts":[[2005,8,1]],"date-time":"2005-08-01T00:52:49Z","timestamp":1122857569000},"page":"385-389","source":"Crossref","is-referenced-by-count":13,"title":["Goldenhar, M\u00f6bius and hypoglossia-hypodactyly anomalies in a patient: Syndrome or association?"],"prefix":"10.1007","volume":"155","author":[{"given":"Sabine","family":"Preis","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Majewski","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Hantschmann","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Schumacher","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H. G.","family":"Lenard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF01955267_CR1","doi-asserted-by":"crossref","first-page":"638","DOI":"10.1212\/WNL.26.7.638","volume":"26","author":"S Aleksic","year":"1976","unstructured":"Aleksic S, Budzilovich G, Choy A, Reuben R, Randt C, Finegold M, McCarthy J, Converse J, Feigin I (1976) Congenital ophthalmoplegia in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome). Neurology 26:638\u2013644","journal-title":"Neurology"},{"key":"BF01955267_CR2","first-page":"285","volume":"11","author":"S Aleksic","year":"1984","unstructured":"Aleksic S, Budzilovich G, Greco MA, MvCarthy J, Reuben R, Margolis S, Epstein F, Feigin I, Pearson J (1984) Intracranial lipomas, hydrocephalus and other CNS anomalies in oculoauriculo-vertebral dysplasia (Goldenhar-Gorlin syndrome). Child Brain 11: 285\u2013297","journal-title":"Child Brain"},{"key":"BF01955267_CR3","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1002\/ajmg.1320470229","volume":"47","author":"JS Bamforth","year":"1993","unstructured":"Bamforth JS (1993) Disruption sequences: embryonic vascular accident or blastogenic disruption sequence? Am J Med Genet 47:284\u2013288","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR4","doi-asserted-by":"crossref","first-page":"415","DOI":"10.1136\/jmg.14.6.415","volume":"14","author":"M Baraitser","year":"1977","unstructured":"Baraitser M (1977) Genetics of M\u00f6bius syndrome. J Med Genet 14:415\u2013417","journal-title":"J Med Genet"},{"key":"BF01955267_CR5","first-page":"287","volume":"26","author":"MK Bassila","year":"1989","unstructured":"Bassila MK, Goldberg R (1989) The association of facial palsy and\/or sensoneural hearing loss in patients with hemifacial microsomia. Cleft Palate J 26:287\u2013291","journal-title":"Cleft Palate J"},{"key":"BF01955267_CR6","doi-asserted-by":"crossref","first-page":"903","DOI":"10.1002\/ajmg.1320230405","volume":"23","author":"JNB Bavinck","year":"1986","unstructured":"Bavinck JNB, Weaver DD (1986) Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and M\u00f6bius anomalies. Am J Med Genet 23:903\u2013918","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR7","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00445029","volume":"122","author":"ET Bersu","year":"1976","unstructured":"Bersu ET, Pettersen JC, Charboneau WJ, Opitz JM (1976) Studies of malformation syndromes of man XXXXI A: anatomical studies in Hanhart syndrome\u2014a pathogenetic hypothesis. Eur J Pediatr 122:1\u201317","journal-title":"Eur J Pediatr"},{"key":"BF01955267_CR8","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1007\/BF00496922","volume":"128","author":"J Bouvet","year":"1978","unstructured":"Bouvet J, Leveque D, Bernetieres F, Gros J (1978) Vascular origin of Poland syndrome? A comparative rheographic study of the vascularisation of the arms in eight patients. Eur J Pediatr 128:17\u201326","journal-title":"Eur J Pediatr"},{"key":"BF01955267_CR9","first-page":"52","volume":"32","author":"B Bretton Chappuis","year":"1989","unstructured":"Bretton Chappuis B, Engel E (1989) Anotie, paralysie faciale, malformations cardiaques: Triade sp\u00e9cifique ou variante du syndrome de Goldenhar? Ann G\u00e9n\u00e9t 32:52\u201354","journal-title":"Ann G\u00e9n\u00e9t"},{"key":"BF01955267_CR10","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1007\/BF00279415","volume":"64","author":"U Burck","year":"1983","unstructured":"Burck U (1983) Genetic aspects of hemifacial microsomia. Hum Genet 64:291\u2013296","journal-title":"Hum Genet"},{"key":"BF01955267_CR11","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1002\/ajmg.1320470230","volume":"47","author":"SS Charles","year":"1993","unstructured":"Charles SS, DiMario FJ, Grunnert ML (1993) M\u00f6bius sequence: further in vivo support for the subclavian artery supply disruption sequence. Am J Med Genet 47:289\u2013293","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR12","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1111\/j.1399-0004.1982.tb01845.x","volume":"22","author":"DL Collins","year":"1982","unstructured":"Collins DL, Schimke RN (1982) Moebius syndrome in a child and extremity defect in her father. Clin Genet 22: 312\u2013314","journal-title":"Clin Genet"},{"key":"BF01955267_CR13","first-page":"866","volume":"52","author":"JL Crosby","year":"1993","unstructured":"Crosby JL, Varnum DS, Nadeau JH (1993) Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation. Am J Hum Genet 52:866\u2013874","journal-title":"Am J Hum Genet"},{"key":"BF01955267_CR14","doi-asserted-by":"crossref","first-page":"882","DOI":"10.1002\/ajmg.1320430526","volume":"43","author":"A David","year":"1992","unstructured":"David A, Roz\u00e9 J, R\u00e9mond S, Branger B, H\u00e9loury Y (1992) Hypoglossiahypodactylia syndrome with jejunal atresia in an infant of a diabetic mother. Am J Med Genet 43:882\u2013884","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR15","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1177\/088307389300800310","volume":"8","author":"N D'Cruz","year":"1993","unstructured":"D'Cruz N, Swisher CN, Jaradeh S, Tang T, Konkol RJ (1993) M\u00f6bius syndrome: evidence for a vascular etiology. J Child Neurol 8:260\u2013265","journal-title":"J Child Neurol"},{"key":"BF01955267_CR16","doi-asserted-by":"crossref","first-page":"762","DOI":"10.1016\/0140-6736(91)91374-4","volume":"337","author":"HV Firth","year":"1991","unstructured":"Firth HV, Boyd PA, Chamberlain P, MacKenzie IZ, Lindenbaum RH, Huson SM (1991) Severe limb abnormalities after chorion villus sampling at 56\u201366 days' gestation. Lancet 337: 762\u2013763","journal-title":"Lancet"},{"key":"BF01955267_CR17","doi-asserted-by":"crossref","first-page":"638","DOI":"10.1001\/archneurpsyc.1919.02180120036004","volume":"2","author":"FR Fry","year":"1919","unstructured":"Fry FR, Kasak M (1919) Congenital facial paralysis. Arch Neurol Psychiatr 2:638\u2013644","journal-title":"Arch Neurol Psychiatr"},{"key":"BF01955267_CR18","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1002\/ajmg.1320470113","volume":"47","author":"CH Gonzalez","year":"1993","unstructured":"Gonzalez CH, Vargas FR, Alvarez Perez AB, Kim CA, Brunoni D, Marques-Dias MJ, Leone CR, Neto JC, Llerena JC, Cabral de Almeida JC (1993) Limb deficiency with or without M\u00f6bius sequence in seven Brazilian children associated with Misoprostol use in the first trimester of pregnancy. Am J Med Genet 47:59\u201364","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR19","doi-asserted-by":"crossref","first-page":"991","DOI":"10.1016\/S0022-3476(63)80233-4","volume":"63","author":"RJ Gorlin","year":"1963","unstructured":"Gorlin RJ, Jue KL, Jacobson U, Goldschmidt E (1963) Oculoauriculovertebral dysplasia. J Pediatr 63:991\u2013999","journal-title":"J Pediatr"},{"key":"BF01955267_CR20","first-page":"641","volume-title":"Syndromes of the head and neck","author":"RJ Gorlin","year":"1990","unstructured":"Gorlin RJ, Cohen MM, Levin LS (1990) Syndromes of the head and neck. 3rd edn. Oxford University Press, New York, pp 641\u2013649, 666\u2013672","edition":"3rd edn."},{"key":"BF01955267_CR21","doi-asserted-by":"crossref","first-page":"570","DOI":"10.1542\/peds.84.3.570","volume":"84","author":"P Govaert","year":"1989","unstructured":"Govaert P, Vanhaesebrouck P, De Praeter C, Fr\u00e4nkel U, Leroy J (1989) Moebius sequence and prenatal brainstem ischemia. Pediatrics 84:570\u2013573","journal-title":"Pediatrics"},{"key":"BF01955267_CR22","first-page":"461","volume":"37","author":"JM Graham","year":"1988","unstructured":"Graham JM, Edwards MJ, Lipson AH, Webster WS (1988) Gestational hyperthermia as a cause for M\u00f6bius syndrome. Teratol 37:461","journal-title":"Teratol"},{"key":"BF01955267_CR23","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1007\/BF01629604","volume":"57","author":"F G\u00fctermann","year":"1917","unstructured":"G\u00fctermann F (1917) Ein Fall von multipler Hirnnervenl\u00e4hmung mit gleichzeitigen Mi\u00dfbildungen am Thorax und an der rechten oberen Extremit\u00e4t. Dtsch Z Nervenheilkd 57:203\u2013224","journal-title":"Dtsch Z Nervenheilkd"},{"key":"BF01955267_CR24","first-page":"2033","volume":"31","author":"H G\u00fctzmann","year":"1905","unstructured":"G\u00fctzmann H (1905) Ein Fall von angeborener Diplegia des Facialis und Abducens. Dtsch Med Wochenschr 31: 2033","journal-title":"Dtsch Med Wochenschr"},{"issue":"No. 7","key":"BF01955267_CR25","first-page":"233","volume":"VII","author":"B Hall","year":"1971","unstructured":"Hall B (1971) Aglossia-adactylia. A case report, review of the literature and classification of closely related entities. Birth Defects Vol. VII, No. 7:233\u2013236","journal-title":"Birth Defects"},{"key":"BF01955267_CR26","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1016\/S0022-3476(85)80710-1","volume":"106","author":"B Hall","year":"1985","unstructured":"Hall B (1985) Anotia, facial paralysis, and heart disease. J Pediatr 106:532","journal-title":"J Pediatr"},{"key":"BF01955267_CR27","doi-asserted-by":"crossref","first-page":"326","DOI":"10.1542\/peds.86.2.326","volume":"86","author":"RCM Hennekam","year":"1990","unstructured":"Hennekam RCM, Hofstee N (1990) Familial liability to intrauterine vascular impairments. Pediatrics 86:326\u2013327","journal-title":"Pediatrics"},{"key":"BF01955267_CR28","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1007\/BF00445030","volume":"122","author":"J Herrmann","year":"1976","unstructured":"Herrmann J, Pallister PD, Gilbert EF, Visekul C, Bersu E, Pettersen JC, Opitz JM (1976) Studies of malformation syndromes of man XXXXI B: nosologic studies in Hanhart and M\u00f6bius syndrome. Eur J Pediatr 122: 19\u201355","journal-title":"Eur J Pediatr"},{"key":"BF01955267_CR29","doi-asserted-by":"crossref","first-page":"839","DOI":"10.1016\/S0022-3476(82)80343-0","volume":"101","author":"HE Hoyme","year":"1982","unstructured":"Hoyme HE, Jones KL, Van Allen MI, Saunders BS, Benirschke K (1982) Vascular pathogenesis of transverse limb reduction defects. J Pediatr 101: 839\u2013843","journal-title":"J Pediatr"},{"key":"BF01955267_CR30","doi-asserted-by":"crossref","first-page":"743","DOI":"10.1542\/peds.85.5.743","volume":"85","author":"HE Hoyme","year":"1990","unstructured":"Hoyme HE, Jones KL, Dixon SD, Jewett T, Hanson JW, Robinson LK, Msall ME, Allanson JE (1990) Prenatal cocaine exposure and fetal vascular disruption. Pediatrics 85:743\u2013747","journal-title":"Pediatrics"},{"key":"BF01955267_CR31","first-page":"212","volume":"23","author":"KP Hummel","year":"1959","unstructured":"Hummel KP (1959) Developmental anomalies in mice resulting from action of the gene, disorganization, a semi-deominant lethal. Pediatrics 23: 212\u2013221","journal-title":"Pediatrics"},{"key":"BF01955267_CR32","unstructured":"Israel JN, Vasan U, Dolezal E, Rubenstein J, Szatkowski M (1987) Goldenhar complex (oculoauricular vertebral anomaly) in an infant of a diabetic: case report. Clinical Genetics Conference Abstracts (Minneapolis): 195"},{"key":"BF01955267_CR33","doi-asserted-by":"crossref","first-page":"12732","DOI":"10.1148\/128.1.127","volume":"128","author":"GF Johnson","year":"1978","unstructured":"Johnson GF, Robinow M (1978) Aglossia-adactylia. Radiology 128: 12732","journal-title":"Radiology"},{"key":"BF01955267_CR34","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1002\/ajmg.1320520403","volume":"52","author":"M Kabra","year":"1994","unstructured":"Kabra M, Suri M, Jain U, Verma IC (1994) Poland anomaly with unusual associated anomalies: case report of an apparent disorganization defect. Am J Med Genet 52:402\u2013405","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR35","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1016\/S0022-3476(76)80456-8","volume":"89","author":"P Kaplan","year":"1976","unstructured":"Kaplan P, Cummings C, Fraser FC (1976) A \u201ccommunity\u201d of face-limb malformation syndromes. J Pediatr 89: 241\u2013247","journal-title":"J Pediatr"},{"key":"BF01955267_CR36","doi-asserted-by":"crossref","first-page":"574","DOI":"10.1002\/ajmg.1320340424","volume":"34","author":"CI Kaye","year":"1989","unstructured":"Kaye CI, Rollnick BR, Hauck WW, Martin AO, Richtsmeier JT, Nagatoshi K (1989) Microtia and associated anomalies: statistical analysis. Am J Med Genet 34:574\u2013578","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR37","doi-asserted-by":"crossref","first-page":"122","DOI":"10.1136\/jmg.27.2.122","volume":"27","author":"D Kumar","year":"1990","unstructured":"Kumar D (1990) Syndrome of the month. Moebius syndrome. J Med Genet 27:122\u2013126","journal-title":"J Med Genet"},{"key":"BF01955267_CR38","unstructured":"Langmann A (1991) Zur Symptomatologie und \u00c4tiologie der Hypoglossie-Hypodaktylie-Assoziation. Dissertation. Heinrich-Heine-Universit\u00e4t D\u00fcsseldorf"},{"key":"BF01955267_CR39","first-page":"77","volume":"31","author":"J Lecannellier","year":"1976","unstructured":"Lecannellier J, Vischer D (1976) Das Aglossie-Adaktylie-Syndrom. Helv Paediatr Acta 31:77\u201384","journal-title":"Helv Paediatr Acta"},{"key":"BF01955267_CR40","first-page":"1223","volume":"49","author":"PM Marden","year":"1966","unstructured":"Marden PM (1966) The syndrome of ankyloglossia superior. Minnesota Med 49:1223\u20131225","journal-title":"Minnesota Med"},{"key":"BF01955267_CR41","doi-asserted-by":"crossref","first-page":"695","DOI":"10.1001\/jama.1966.03100080135048","volume":"195","author":"F Matthies","year":"1966","unstructured":"Matthies F (1966) The triad of anotia, facial paralysis, and cardiac anomaly not due to Thalidomide. JAMA 195: 695\u2013696","journal-title":"JAMA"},{"key":"BF01955267_CR42","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1136\/adc.33.171.477","volume":"33","author":"J McKenzie","year":"1958","unstructured":"McKenzie J (1958) The first arch syndrome. Arch Dis Child 33:477\u2013486","journal-title":"Arch Dis Child"},{"key":"BF01955267_CR43","first-page":"1","volume":"2","author":"JM Opitz","year":"1986","unstructured":"Opitz JM (1986) Developmental field theory and observations-accidental progress? Am J Med Genet Supp 2: 1\u20138","journal-title":"Am J Med Genet Supp"},{"key":"BF01955267_CR44","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1016\/S0140-6736(65)91073-1","volume":"I","author":"E Passarge","year":"1965","unstructured":"Passarge E (1965) Congenital malformations and maternal diabetes. Lancet I:324","journal-title":"Lancet"},{"key":"BF01955267_CR45","doi-asserted-by":"crossref","first-page":"441","DOI":"10.1016\/S0022-3476(84)80025-6","volume":"105","author":"W Pearl","year":"1984","unstructured":"Pearl W (1984) Syndrome of anotia, facial paralysis, and congenital heart disease. J Pediatr 105:441\u2013442","journal-title":"J Pediatr"},{"key":"BF01955267_CR46","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1007\/BF02426976","volume":"2","author":"MEM Pierpont","year":"1982","unstructured":"Pierpont MEM, Moller JH, Gorlin RJ, Edwards JE (1982) Congenital cardiac, pulmonary, and vascular malformations in oculoauriculovertebral dysplasia. Pediatr Cardiol 2:297\u2013302","journal-title":"Pediatr Cardiol"},{"key":"BF01955267_CR47","doi-asserted-by":"crossref","first-page":"302","DOI":"10.1016\/0030-4220(73)90070-4","volume":"35","author":"D Poswillo","year":"1973","unstructured":"Poswillo D (1973) The pathogenesis of the first and second branchial arch syndrome. Oral Surg 35:302\u2013329","journal-title":"Oral Surg"},{"key":"BF01955267_CR48","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1111\/j.1399-0004.1982.tb00957.x","volume":"21","author":"L Regenbogen","year":"1982","unstructured":"Regenbogen L, Godel V, Goodman RM (1982) Further evidence for autosomal dominant form of oculoauriculovertebral dysplasia. Clin Genet 21:161\u2013167","journal-title":"Clin Genet"},{"key":"BF01955267_CR49","doi-asserted-by":"crossref","first-page":"236","DOI":"10.1016\/S0022-3476(87)80074-4","volume":"11","author":"LK Robinson","year":"1987","unstructured":"Robinson LK, Hoyme HE, Edwards DK, Jones KL (1987) Vascular pathogenesis of unilateral craniofacial defects. J Pediatr 11:236\u2013239","journal-title":"J Pediatr"},{"key":"BF01955267_CR50","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1002\/ajmg.1320470115","volume":"47","author":"JI Rodr\u00edguez","year":"1993","unstructured":"Rodr\u00edguez JI, Palacios J, Lapunzina P (1993) Severe axial anomalies in the oculo-auriculo-vertebral (Goldenhar) complex. Am J Med Genet 47:69\u201374","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR51","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1002\/ajmg.1320150207","volume":"15","author":"BR Rollnick","year":"1983","unstructured":"Rollnick BR, Kaye CI (1983) Hemifacial microsomia and variants: Predigree Data. Am J Med Genet 15:233\u2013253","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR52","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1002\/ajmg.1320260215","volume":"26","author":"BR Rollnick","year":"1987","unstructured":"Rollnick BR, Kaye CI, Nagatoshi K, Martin A (1987) Oculoauriculovertebral dysplasia and variants: Phenotypic characteristics of 294 patients. Am J Med Genet 26:361\u2013375","journal-title":"Am J Med Genet"},{"key":"BF01955267_CR53","first-page":"51","volume-title":"Treatment of hemifacial microsomia","author":"L Samuels","year":"1993","unstructured":"Samuels L, Lawson LI, Rowe LD (1993) Characteristics of patients with hemifacial microsomia at the craniofacial center. In: Harvold EP (ed) Treatment of hemifacial microsomia. Alan Liss, New York, pp 51\u201355"},{"key":"BF01955267_CR54","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1016\/S0022-3476(79)80278-4","volume":"95","author":"AAGL Schinzel","year":"1979","unstructured":"Schinzel AAGL, Smith DW, Miller JR (1979) Monozygotic twinning and structural defects. J Pediatr 95:921\u2013930","journal-title":"J Pediatr"},{"key":"BF01955267_CR55","first-page":"151","volume":"6","author":"Z Smakel","year":"1986","unstructured":"Smakel Z (1986) Craniofacial changes in hemifacial microsomia. J Craniofac Genet Develop Biol 6:151\u2013170","journal-title":"J Craniofac Genet Develop Biol"},{"key":"BF01955267_CR56","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1016\/S0022-3476(86)80783-1","volume":"108","author":"HC Soltan","year":"1986","unstructured":"Soltan HC, Holmes LB (1986) Familial occurrence of malformations possibly attributable to vascular abnormalities. J Pediatr 108:112\u2013114","journal-title":"J Pediatr"},{"key":"BF01955267_CR57","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1002\/ajmg.1320460325","volume":"46","author":"FJ Stewart","year":"1993","unstructured":"Stewart FJ, Boston VE (1993) Poland anomaly with a limb body wall disruption defect. Am J Med Genet 46:350","journal-title":"Am J Med Genet"},{"issue":"No. 3","key":"BF01955267_CR58","first-page":"125","volume":"V","author":"S Temtamy","year":"1969","unstructured":"Temtamy S, McKusick VA (1969) Synopsis of hand malformations with particular emphasis on genetic factors. Birth Defects Vol. V, No. 3:125\u2013184","journal-title":"Birth Defects"},{"key":"BF01955267_CR59","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1111\/j.1399-0004.1977.tb01338.x","volume":"11","author":"E Tuncbilek","year":"1977","unstructured":"Tuncbilek E, Yalcin C, Atasu M (1977) Aglossia-adactylia syndrome (special emphasis on the inheritance pattern). Clin Genet 11:421\u2013423","journal-title":"Clin Genet"},{"key":"BF01955267_CR60","first-page":"199","volume":"38","author":"WS Webster","year":"1988","unstructured":"Webster WS, Lipson AH, Brown-Woodman PDC, Osborn RA (1988) Moebius unmasked: pathogenesis of the Moebius syndrome in an animal model. Teratology 38:199","journal-title":"Teratology"}],"container-title":["European Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01955267.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF01955267\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01955267","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,1,28]],"date-time":"2024-01-28T10:06:42Z","timestamp":1706436402000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF01955267"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,5]]},"references-count":60,"journal-issue":{"issue":"5","published-print":{"date-parts":[[1996,5]]}},"alternative-id":["BF01955267"],"URL":"https:\/\/doi.org\/10.1007\/bf01955267","relation":{},"ISSN":["0340-6199","1432-1076"],"issn-type":[{"value":"0340-6199","type":"print"},{"value":"1432-1076","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,5]]}}}