通过Q带和G带模式鉴定家族性19 - 21易位 - Suppr

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Identification of a familial 19-21 translocation by Q and G band patterns.

作者信息

Vogel W, Löning B

出版信息

Humangenetik. 1973 May 25;18(3):219-24. doi: 10.1007/BF00290600.

DOI:10.1007/BF00290600

PMID:4719633

Abstract

摘要

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本文引用的文献

[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].

Ann Genet. 1966;9(1):12-8.

A simplified method of demonstrating Giemsa-band pattern in human chromosomes.

Humangenetik. 1971;14(1):83-4. doi: 10.1007/BF00273042.

Ring formation of chromosomes nos. 19 and 20.

Cytogenetics. 1972;11(3):208-15. doi: 10.1159/000130190.

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

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

Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

Clin Genet. 1972;3(4):226-48. doi: 10.1111/j.1399-0004.1972.tb04271.x.

Maternal transmission of a 21/1 translocation associated with Down's syndrome.

J Pediatr. 1966 Oct;69(4):635-9. doi: 10.1016/s0022-3476(66)80052-5.

Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.

Humangenetik. 1971;12(1):67-73. doi: 10.1007/BF00291036.

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