通过G带模式鉴定克氏综合征的18 - 21易位 - Suppr

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Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.

作者信息

Waldenmaier C, Hirsch W, König E, Shibata K

出版信息

Humangenetik. 1974 Mar 28;21(4):323-9. doi: 10.1007/BF00273370.

DOI:10.1007/BF00273370

PMID:4134628

Abstract

摘要

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Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.通过G带模式鉴定克氏综合征的18 - 21易位

Humangenetik. 1974 Mar 28;21(4):323-9. doi: 10.1007/BF00273370.

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Presumptive Y-15 translocation and mental retardation in a family with a case of Klinefelter's syndrome.一个患有克兰费尔特综合征病例的家族中推测的Y-15易位与智力迟钝。

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引用本文的文献

Constitutional complex chromosomal rearrangements in a klinefelter patient: case report and review of literature.克氏综合征患者的复杂染色体结构重排：病例报告及文献复习。

J Assist Reprod Genet. 2012 May;29(5):437-41. doi: 10.1007/s10815-012-9725-y. Epub 2012 Mar 1.

A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent.一名患有头面正中畸形的46,XY,del(18)(pter至p1 100:）患儿，其父母一方核型为正常的46,XX,t(12;18)(18pter至18 p 1100:: 12qter至12pter) 。

Hum Genet. 1976 Sep 10;34(1):103-6. doi: 10.1007/BF00284446.

本文引用的文献

The use of perforated cellophane for the growth of cells in tissue culture.在组织培养中使用穿孔玻璃纸促进细胞生长。

J Natl Cancer Inst. 1947 Dec;8(3):103-19.

MICROTECHNIQUE FOR CULTURING LEUKOCYTES FROM WHOLE BLOOD.从全血中培养白细胞的显微技术。

Cytogenetics. 1963;2:57-60. doi: 10.1159/000129767.

Dicentric chromosome due to an unusual fusion.由于异常融合导致的双着丝粒染色体。

Humangenetik. 1971;12(2):136-41. doi: 10.1007/BF00291469.

Topological classification of palmar dermatoglyphics.

J Ment Defic Res. 1970 Jun;14(2):111-28. doi: 10.1111/j.1365-2788.1970.tb01106.x.

Dermatoglyphic sole patterns. a new attempt at classification.足底皮纹模式。一种分类的新尝试。

Hum Biol. 1969 Sep;41(3):427-48.

[Short-arm deletion of chromosome 18 due to a t(G-;18p+) translocation. Fluorescence study with quinacrine mustard].因t（G-；18p+）易位导致的18号染色体短臂缺失。用喹吖因氮芥进行荧光研究

Ann Genet. 1971 Sep;14(3):213-8.

[Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism].[18号染色体短臂完全缺失及G-18易位伴色素异常和甲状腺功能减退]

Arch Fr Pediatr. 1971 Oct;28(8):837-46.

[Ring chromosome 18. 18p-/18q- -deletion-syndrome].[环状染色体18。18p - /18q - 缺失综合征]

Humangenetik. 1972;15(4):289-318. doi: 10.1007/BF00281730.

Partial monosomies 18. Review of cytogenetical and phenotypical variants.18号染色体部分单体性。细胞遗传学和表型变异综述。

Humangenetik. 1972;15(3):203-22. doi: 10.1007/BF00702354.

A rapid banding technique for routine use in human and comparative cytogenetics.一种用于人类和比较细胞遗传学常规检测的快速显带技术。

Humangenetik. 1972;15(4):349-53. doi: 10.1007/BF00281736.

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