唇顎口蓋裂を伴った18長腕部分欠失症の一例
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Published in | 小児口腔外科 Vol. 1; no. 2; pp. 118 - 123 |
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Main Authors | , , , |
Format | Journal Article |
Language | Japanese |
Published |
日本小児口腔外科学会
30.11.1991
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Subjects | |
Online Access | Get full text |
ISSN | 0917-5261 1884-6661 |
DOI | 10.11265/poms1991.1.118 |
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Author | 別府, 和紀 岩崎, 誠 竹之下, 康治 岡, 増一郎 |
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References | 7) Mertelecki, W. et al.: Partial deletion of chromosome 18. Lancet 2: 641 1966. 8) Dziba, P. J. et al.: Famillial occurence of deletion of long arm of chromosome 18. (46, 18q-). Pediat. Pol. 47: 1037-1042 1972. 3) Bergsma, D.: Birth defects compendium (2nd Ed.), Alan R Liss, New. York, 1979, p200-201. 5) 阿部達生, 藤田弘子: 染色体アトラス. 南江堂, 東京, 1981, 8-10頁. 12) 平瀬雄一, 他: 第18環状染色体児の1例. 形成外科 39: 448-453 1986. 9) Wilson, M. G. et al.: Syndromes associated with deletion of the long arm of chromosome 18 [del (18q) ]. Am. J. Med. Genet. 3: 155-174 1979. 11) 月野隆一: 1. 染色体異常. 18q-症候群. 日本臨床 45: 52 1987. 6) Schinzel, K. et al.: Structural aberrations of chromosome 18. The 18q-syndrome. Report of three cases. Human Genet. 26: 123-132 1975. 1) de Grouchy, J. R. et al.: Deletion partielle des bars longs du chromosome 18. Path. Biol. 12: 579-582 1964. 2) 松井一郎: 小児科における先天性および遺伝性の疾患. 小児科診療 50: 562-571 1987. 4) 池田恵一: ベッドサイドの小児外科. 南山堂, 東京, 1979, 253頁. 10) Feingold, M. et al.: Ig-A deficiency associated with partial deletion of chromosome 18. Am. J. Dis. Child. 117: 129-136 1969. 13) 柳沢慧: 18およびD1トリソミー症候群. 小児医学 6: 65-105 1973. |
References_xml | – reference: 7) Mertelecki, W. et al.: Partial deletion of chromosome 18. Lancet 2: 641 1966. – reference: 9) Wilson, M. G. et al.: Syndromes associated with deletion of the long arm of chromosome 18 [del (18q) ]. Am. J. Med. Genet. 3: 155-174 1979. – reference: 12) 平瀬雄一, 他: 第18環状染色体児の1例. 形成外科 39: 448-453 1986. – reference: 5) 阿部達生, 藤田弘子: 染色体アトラス. 南江堂, 東京, 1981, 8-10頁. – reference: 10) Feingold, M. et al.: Ig-A deficiency associated with partial deletion of chromosome 18. Am. J. Dis. Child. 117: 129-136 1969. – reference: 4) 池田恵一: ベッドサイドの小児外科. 南山堂, 東京, 1979, 253頁. – reference: 11) 月野隆一: 1. 染色体異常. 18q-症候群. 日本臨床 45: 52 1987. – reference: 2) 松井一郎: 小児科における先天性および遺伝性の疾患. 小児科診療 50: 562-571 1987. – reference: 3) Bergsma, D.: Birth defects compendium (2nd Ed.), Alan R Liss, New. York, 1979, p200-201. – reference: 8) Dziba, P. J. et al.: Famillial occurence of deletion of long arm of chromosome 18. (46, 18q-). Pediat. Pol. 47: 1037-1042 1972. – reference: 6) Schinzel, K. et al.: Structural aberrations of chromosome 18. The 18q-syndrome. Report of three cases. Human Genet. 26: 123-132 1975. – reference: 1) de Grouchy, J. R. et al.: Deletion partielle des bars longs du chromosome 18. Path. Biol. 12: 579-582 1964. – reference: 13) 柳沢慧: 18およびD1トリソミー症候群. 小児医学 6: 65-105 1973. |
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SubjectTerms | 18q部分モノソミー症候群 両側性口唇裂・口蓋裂 免疫グロブリン |
Title | 唇顎口蓋裂を伴った18長腕部分欠失症の一例 |
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