A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13)etc. In a male infant
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/jhg19865.pdf
Reference10 articles.
1. Bourgeois, C.A. 1974. Distribution of mitomycin C-induced damage in human chromosomes with special reference to regions of repetitive DNA.Chromosoma 48:203–211.
2. Brøgger, A. and Johansen, J. 1972. A model for the production of chromosome damage by mitomycin C.Chromosoma 38:95–104.
3. Cohen, M.M., Rosenmann, A., Hacham-Zadeh, S., and Dahan, S. 1975. Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv(2) (p15q21)] in a patient with gonadal dysgenesis.Clin. Genet. 8:11–17.
4. Dewald, G.W., Boros, S.J., Conroy, M.M., Dahl, R.J., Spurbec, J.L., and Vitec, H.A. 1979. A tdic(5;15)(p13;p11) chromosome showing variation for constriction in the centromeric regions in a patient with the cri du chat syndrome.Cytogenet. Cell Genet. 24:15–26.
5. Distéche, C., Hagemeijer, A., Frederic, J., and Progneaux, D. 1972. 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.Clin. Genet. 3:388–395.
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1. Nonreciprocal and jumping translocations of 15q1→qter in Prader-Willi syndrome;American Journal of Medical Genetics;1990-11
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