참고문헌 (15)

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2. 2 Paez MT Yamamoto T Hayashi K Yasuda T Harada N Matsumoto N Two patients with atypical interstitial deletions of 8p23.1: Mapping of phenotypical traits Am J Med Genet A 2008 146A 1158 1165 18393291 

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5. 5 de Vries BB Lees M Knight SJ Regan R Corney D Flint J Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13) Am J Med Genet 2001 99 314 319 11251999 

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6. 6 Barber JC Maloney VK Huang S Bunyan DJ Cresswell L Kinning E 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array cgh Eur J Hum Genet 2008 16 18 27 17940555 

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7. 7 Pettenati MJ Rao N Johnson C Hayworth R Crandall K Huff O Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation Hum Genet 1992 89 602 606 1511976 

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8. 8 Claeys I Holvoet M Eyskens B Adriaensens P Gewillig M Fryns JP A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8 Am J Med Genet 1997 74 515 520 9342203 

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9. 9 Hutchinson R Wilson M Voullaire L Distal 8p deletion (8p23.1----8pter): A common deletion? J Med Genet 1992 29 407 411 1619636 

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10. 10 Devriendt K De Mars K De Cock P Gewillig M Fryns JP Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome Ann Genet 1995 38 228 230 8629811 

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11. 11 Fernandez-Garcia R Perez Mencia T Gutierrez-Jodra A Lopez Garcia A Anesthetic management with laryngeal mask in a child with brachmann-de lange syndrome Paediatr Anaesth 2006 16 698 700 16719891 

12. 12 Tsukazaki Y Tachibana C Satoh K Fukada T Ohe Y A patient with cornelia de lange syndrome with difficulty in orotracheal intubation Masui 1996 45 991 993 8818097 

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13. 13 Corsini LM De Stefano G Porras MC Galindo S Palencia J Anaesthetic implications of cornelia de lange syndrome Paediatr Anaesth 1998 8 159 161 9549745 

14. 14 Cormack RS Lehane J Difficult tracheal intubation in obstetrics Anaesthesia 1984 39 1105 1111 6507827 

15. 15 Giglio S Graw SL Gimelli G Pirola B Varone P Voullaire L Deletion of a 5-cm region at chromosome 8p23 is associated with a spectrum of congenital heart defects Circulation 2000 102 432 437 10908216 

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