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 - Suppr

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超能文献

[Short-arm deletion of chromosome 18 due to a t(G-;18p+) translocation. Fluorescence study with quinacrine mustard].

作者信息

Malpuech G, Raynaud E J, Belin J, Godeneche P, de Grouchy J

出版信息

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

PMID:5315468

Abstract

摘要

相似文献

[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.

[Deletion of the short arm of chromosome 18 due to t(22-;18p+) translocation with IgA deficiency. Cytogenetic study with autoradiography and fluorescence].

Ann Genet. 1972 Dec;15(4):275-81.

[Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism].

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

[The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].[18号染色体短臂缺失（18p-综合征），基于一项新观察]

Ann Genet. 1968 Mar;11(1):17-21.

[A recent case of partial deletion of short arm of chromosome 18].

Ann Genet. 1970 Jun;13(2):120-2.

Chromatid interchange resulting in duplication of the short arm of chromosome number 7 in man.

Ann Genet. 1971 Jun;14(2):143-4.

A case with short arm deletion of chromosome 18 (18p-syndrome).

Jinrui Idengaku Zasshi. 1973 Jun;18(1):24-36.

A case of 18q- in a t(18q-;6p+) family.一个携带t(18q-;6p+)的家族中出现的18号染色体长臂缺失病例。

Ann Genet. 1971 Mar;14(1):41-8.

[Identification of several chromosome aberrations in man by the fluorescent method using quinacrine yprite].[利用喹吖因芥子气荧光法鉴定人类的几种染色体畸变]

Tsitologiia. 1976 Feb;18(2):213-8.

[18p- syndrome. A further case].[18p-综合征。又一例病例]

Ann Genet. 1969 Jun;12(2):122-5.

引用本文的文献

[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.

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.

The use of new staining techniques for human chromosome identification.用于人类染色体识别的新染色技术的应用。

J Med Genet. 1972 Sep;9(3):264-75. doi: 10.1136/jmg.9.3.264.

18p--syndrome resulting from 14q/18q 'dicentric' fusion translocation.由14号染色体长臂/18号染色体长臂“双着丝粒”融合易位导致的18号染色体短臂缺失综合征

Hum Genet. 1977 Nov 10;39(2):243-50. doi: 10.1007/BF00287020.

Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.人类中的相互易位。3:1减数分裂分离导致产生47条或45条染色体的后代。

J Med Genet. 1975 Mar;12(1):29-43. doi: 10.1136/jmg.12.1.29.

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