Branchio-Oto-Renal Syndromeの一症例
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| Published in | 小児耳鼻咽喉科 Vol. 13; no. 1; pp. 43 - 44 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | Japanese |
| Published |
日本小児耳鼻咽喉科学会
1992
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| Online Access | Get full text |
| ISSN | 0919-5858 2186-5957 |
| DOI | 10.11374/shonijibi1980.13.1_43 |
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| Author | 市村, 恵一 横小路, 雅文 加藤, 昌樹 郭, 宗佐 |
|---|---|
| Author_xml | – sequence: 1 fullname: 横小路, 雅文 organization: 柏厚生病院耳鼻咽喉科, 東京大学耳鼻咽喉科 – sequence: 1 fullname: 市村, 恵一 organization: 東京大学分院耳鼻咽喉科 – sequence: 1 fullname: 加藤, 昌樹 organization: 関東労災病院耳鼻咽喉科 – sequence: 1 fullname: 郭, 宗佐 organization: 武蔵野赤十字病院耳鼻咽喉科 |
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| References | 9)神野和彦, 田辺明男, 松浦良二: Branchio-oto-Renal Syndrom の一症例. 小児科臨床40: 675-679, 1987. 3) Fraser FC, Sproule JR, Halal F: Frequency of the branchiooto-renal (BOR) syndrome in children with pro found hearing loss. Am J Med Genet 7: 341-349, 1980. 5) Melnick M, Bixler D, Nance WE, et al: Familal branchiootorenal dysplasia: A new addition to the branchial arch syndromes. Clin Genet 9: 25-34, 1976. 6) Melnick M, Hodes ME, Nance WE, et al: Branchio-Otorenal dysplasia and Branchio-oto dysplasia: Tw o distinct autosomal dominant disorders. Clin Genet 13: 425-442, 197 8. 8)市村恵一, 芹沢康博, 宮下弘, 和田芳弘, 星野知之: Branchio-oto-Renal Syndromo -症例報告と疾患概念の検討-. 耳鼻31; 959-966, 1985. 2) Melnick M, Bixler D, Silk KS, Une H, Nance W,: Autosomal dominance of branchio-renal dysplasia. In “N ew Chromosomal and Malformation Syndrome (1974 Birth Defects Conference). ” Miami: Symposia Specialists for The National Foundation-March of Dimes. BD: OAS XI: 1 21-128, 1975. 7) Gimsing S, Dyrmose J: Branchio-oto-renal dysplasia in three families. An Otol Rhinol Laryngol 95: 421-426. 1986. 1) Cremers CWRJ, Fikkers-Von Noord M: The earnits-deafness syndrome. Clinical and genetic aspects. Int ernational J Pediatric Otorhinolaryngol. 2: 309-322, 1980. 10) Smith PG, Dyches TJ, Loomis RA: Clinical aspects of the b9r2anchio-otorenal syndrome. Otolaryngol Head Neck Surg, 92: 468-475, 1984. 4) Fraser FC, Ling D, Clogg D, Nogrady B: Gnetic aspects of the BOR Syndrome-Branchial fistulas, earpits, hearing los s, and renal anomalies. Am J Med Genet 2: 241-252, 1978. |
| References_xml | – reference: 10) Smith PG, Dyches TJ, Loomis RA: Clinical aspects of the b9r2anchio-otorenal syndrome. Otolaryngol Head Neck Surg, 92: 468-475, 1984. – reference: 7) Gimsing S, Dyrmose J: Branchio-oto-renal dysplasia in three families. An Otol Rhinol Laryngol 95: 421-426. 1986. – reference: 5) Melnick M, Bixler D, Nance WE, et al: Familal branchiootorenal dysplasia: A new addition to the branchial arch syndromes. Clin Genet 9: 25-34, 1976. – reference: 9)神野和彦, 田辺明男, 松浦良二: Branchio-oto-Renal Syndrom の一症例. 小児科臨床40: 675-679, 1987. – reference: 4) Fraser FC, Ling D, Clogg D, Nogrady B: Gnetic aspects of the BOR Syndrome-Branchial fistulas, earpits, hearing los s, and renal anomalies. Am J Med Genet 2: 241-252, 1978. – reference: 8)市村恵一, 芹沢康博, 宮下弘, 和田芳弘, 星野知之: Branchio-oto-Renal Syndromo -症例報告と疾患概念の検討-. 耳鼻31; 959-966, 1985. – reference: 6) Melnick M, Hodes ME, Nance WE, et al: Branchio-Otorenal dysplasia and Branchio-oto dysplasia: Tw o distinct autosomal dominant disorders. Clin Genet 13: 425-442, 197 8. – reference: 2) Melnick M, Bixler D, Silk KS, Une H, Nance W,: Autosomal dominance of branchio-renal dysplasia. In “N ew Chromosomal and Malformation Syndrome (1974 Birth Defects Conference). ” Miami: Symposia Specialists for The National Foundation-March of Dimes. BD: OAS XI: 1 21-128, 1975. – reference: 1) Cremers CWRJ, Fikkers-Von Noord M: The earnits-deafness syndrome. Clinical and genetic aspects. Int ernational J Pediatric Otorhinolaryngol. 2: 309-322, 1980. – reference: 3) Fraser FC, Sproule JR, Halal F: Frequency of the branchiooto-renal (BOR) syndrome in children with pro found hearing loss. Am J Med Genet 7: 341-349, 1980. |
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| Title | Branchio-Oto-Renal Syndromeの一症例 |
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