Letter: Confirmation of trisomy 22 with fluorescence banding.
作者信息
Uchida I A, Byrnes E M
出版信息
Am J Hum Genet. 1976 Mar;28(2):189-90.
Abstract
摘要
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Letter: Confirmation of trisomy 22 with fluorescence banding.信函：通过荧光带型分析确认22三体综合征
Am J Hum Genet. 1976 Mar;28(2):189-90.
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引用本文的文献
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Tertiary trisomy (22q11q),47,+der(22),t(11;22).三级三体（22q11q），47，+der(22)，t(11;22)
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Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism.基因丰富的染色体区域与常染色体三体性。一例3号染色体三体性嵌合体病例。
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47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.47，XY，+der(11;22)(q23;q12)，继发于母系平衡易位t(11;22)(q23;q12)。关于22三体问题的评论。
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A case of trisomy 22 with a probable Robertsonian translocation 21/22.一例22三体综合征，可能存在21/22罗伯逊易位。
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Trisomy 22 with 'cat eye' anomaly.伴有“猫眼”异常的22三体综合征。
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本文引用的文献
1
Familial occurrence of trisomy 22.22三体综合征的家族性发生情况。
Am J Hum Genet. 1968 Mar;20(2):107-18.
2
Trisomy 22: a clinical entity.22三体综合征：一种临床病症。
J Pediatr. 1971 Jul;79(1):12-9. doi: 10.1016/s0022-3476(71)80052-5.
3
Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding.通过荧光和胰酶吉姆萨带型鉴定出可能的22号染色体三体。
Ann Genet. 1973 Sep;16(3):189-92.
4
Tritiated thymidine uptake by group G chromosomes of female individuals with Down's syndrome.
Exp Cell Res. 1966 Aug;43(1):210-3. doi: 10.1016/0014-4827(66)90393-4.
5
XO-XX-XXX mosaicism with Turner stigmata.具有特纳氏征的XO-XX-XXX嵌合体
Lancet. 1967 Jun 3;1(7501):1228-9. doi: 10.1016/s0140-6736(67)92880-2.
6
Trisomy 22. Two new cases and delineation of the phenotype.22三体综合征。两例新病例及表型描述。
J Med Genet. 1975 Jun;12(2):193-9. doi: 10.1136/jmg.12.2.193.
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