An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry-Reference-Cited by-同舟云学术

An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry

Published:2008-04-23 Issue:5 Volume:3 Page:388-395
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Distèche C.,Hagemeuer A.,Frederic J.,Prqgneaux D.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1972.tb01472.x/fullpdf

Reference18 articles.

1. Familial translocation involving chromosomes6, 14 and 20, identified by quinacrine fluorescence;Allderdice;Hum. Genet.,1971

2. Localization of heterochromatin in human chromosomes;Arrighi;Cytogenetics,1971

3. The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities;Bobrow;J. med. Genet.,1971

4. Identification of human chromosomes by DNA-binding fluorescent agents;Caspersson;Chromosoma (Berl.),1970a

5. The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis;Caspersson;Hereditas (Lund),1970b

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