一名儿童因母亲染色体11、12和13的复杂重排而导致11号染色体部分三体。 - Suppr

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超能文献

Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.

作者信息

Sanchez O, Yunis J J, Escobar J I

出版信息

Humangenetik. 1974 Apr 24;22(1):59-65. doi: 10.1007/BF00338135.

DOI:10.1007/BF00338135

PMID:4134840

Abstract

摘要

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Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.一名儿童因母亲染色体11、12和13的复杂重排而导致11号染色体部分三体。

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A familial reciprocal translocation between three chromosomes.三条染色体之间的家族性相互易位。

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本文引用的文献

Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl.从小量全血接种物培养白细胞，并通过用低渗氯化钾处理制备中期染色体。

Stain Technol. 1965 Nov;40(6):333-8. doi: 10.3109/10520296509116440.

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.人染色体的喹吖因氮芥荧光：异常易位的特征

Am J Hum Genet. 1972 Mar;24(2):189-213.

A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10.一种由10号染色体长臂远端三分之一部分三体性导致的新综合征。

J Pediatr. 1974 Apr;84(4):567-70. doi: 10.1016/s0022-3476(74)80683-9.

Partial trisomy of chromosome 11: a case report.11号染色体部分三体：一例报告

Am J Ment Defic. 1973 Jan;77(4):383-8.

Partial trisomy of 7q resulting from a familial translocation.由家族性易位导致的7号染色体长臂部分三体。

Ann Genet. 1973 Mar;16(1):51-4.

Precise identification of various chromosomal abnormalities.精确识别各种染色体异常。

Ann Hum Genet. 1973 Apr;36(4):375-9. doi: 10.1111/j.1469-1809.1973.tb00601.x.

G-banding and chromosome structure.

Chromosoma. 1973;44(1):15-23. doi: 10.1007/BF00372570.

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].9号染色体短臂三体的吉姆萨R显带分析及1例新病例报告

Humangenetik. 1973 Apr 16;18(2):129-38. doi: 10.1007/BF00291480.

Identification of partial 12 trisomy by quinacrine fluorescence.用喹吖因荧光法鉴定部分12三体

J Pediatr. 1973 Feb;82(2):269-72. doi: 10.1016/s0022-3476(73)80165-9.

Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.通过荧光和吉姆萨显带技术鉴定出4例8三体患者。

J Med Genet. 1972 Mar;9(1):1-7. doi: 10.1136/jmg.9.1.1.

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