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The C syndrome of multiple congenital anomalies
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The C syndrome of multiple congenital anomalies. JM Opitz RC Johnson SR Mc Creadie DW Smith, Birth Defects, Original Article Series New York: The National Foundation, Bergsma D, 1969 2 161 166
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Opitz, J.M.1
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Further delineation of the C (trigonocephaly) syndrome
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DOI 10.1002/ajmg.1320090209
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Further delineation of the C (trigonocephaly) syndrome. RM Antley DS Hwang W Theopold, Am J Med Genet 1981 9 147 163 10.1002/ajmg.1320090209 7258228 (Pubitemid 11112537)
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Antley, R.M.1
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Mortality and pathological findings in C (Opitz trigonocephaly) syndrome
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Mortality and pathological findings in C (Opitz trigonocephaly) syndrome. JM Opitz AR Putnam JM Comstock S Chin JL Byrne A Kennedy MJ Frikke C Bernard S Albrecht V Der Kaloustian JG Szakacs, Fetal Pediatr Pathol 2006 25 211 231 10.1080/15513810601015753 17162528 (Pubitemid 44949938)
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Opitz, J.M.1
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'C' trigonocephaly syndrome: Clinical variability and possibility of surgical treatment
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"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment. F Lalatta D Clerici Bagozzi MG Salmoiraghi P Tagliabue C Tischer M Zollino C Di Rocco G Neri JM Opitz, Am J Med Genet 1990 37 451 456 10.1002/ajmg.1320370404 2260586 (Pubitemid 20380822)
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Clinical and genetic aspects of trigonocephaly: A study of 25 cases
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Clinical and genetic aspects of trigonocephaly: a study of 25 cases. C Azimi SJ Kennedy D Chitayat P Chakraborty JT Clarke C Forrest AS Teebi, Am J Med Genet A 2003 117A 127 135 12567409 (Pubitemid 37064006)
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Opitz trigonocephaly C syndrome associated with hearing loss
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Opitz trigonocephaly C syndrome associated with hearing loss. E Nacarküçük M Okan H Sarimehmet T Ozer, Pediatr Int 2003 45 731 733 10.1111/j.1442-200X.2003.01819.x 14651551 (Pubitemid 38130371)
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Opitz C trigonocephaly syndrome and midline brain anomalies
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Opitz C trigonocephaly syndrome and midline brain anomalies. G Zampino C Di Rocco G Butera, Am J Med Genet 1997 73 484 488 10.1002/(SICI)1096- 8628(19971231)73:4<484::AID-AJMG20>3.0.CO;2-M 9415479 (Pubitemid 27514795)
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Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome
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DOI 10.1086/522014
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Mutations in CD96, a Member of the Immunoglobulin Superfamily, Cause a Form of the C (Opitz Trigonocephaly) Syndrome. T Kaname K Yanagi Y Chinen Y Makita N Okamoto H Maehara I Owan F Kanaya Y Kubota Y Oike T Yamamoto K Kurosawa Y Fukushima A Bohring JM Opitz K Yoshiura N Niikawa K Naritomi, Am J Med Genet A 2007 81 835 841 (Pubitemid 47596551)
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Kaname, T.1
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Maehara, H.6
Owan, I.7
Kanaya, F.8
Kubota, Y.9
Oike, Y.10
Yamamoto, T.11
Kurosawa, K.12
Fukushima, Y.13
Bohring, A.14
Opitz, J.M.15
Yoshiura, K.-I.16
Niikawa, N.17
Naritomi, K.18
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