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Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1) Cover

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

Open Access
|Jul 2011

References

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  9. Kondo I, Hamaguchi H, Matsuura A, Nakajima H, Koyama A, Takita H. A case of Turner's syndrome with familial balanced translocation t(1;2)(q32;q21)mat. J Med Genet. 1979; 16(4): 321-323.10.1136/jmg.16.4.3211012681490589
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  11. Benn PA, Perle MA. Chromosome staining and banding techniques. In: Rooney DE, Czepulkowski BH, Eds. Human Cytogenetics: A Practical Approach, Vol. I. Constitutional Analysis. Oxford: IRL Press Ltd. 1992: 91-118.
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  13. Ruibal Francisco JL, Sánchez Burón P, Piñero Martinez E, Bueno Lozano G, Reverte Blanc F. Turner's syndrome. Relationship between the karyotypes and malformations and associated diseases in 23 patients. An Esp Pediatr. 1997; 47(2): 167-171.
  14. James RS, Dalton P, Gustashaw K, Wolff DJ, Willard HF, Mitchell C, Jacobs PA. Molecular characterization of isochromosomes of Xq. Ann Hum Genet. 1997; 61(Part 6): 485-990.10.1017/S0003480097006519
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Language: English
Page range: 57 - 60
Published on: Jul 25, 2011
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2011 Z Cetin, I Mendilcioglu, S Yakut, S Berker-Karauzum, B Karaman, G Luleci, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons License.

Volume 14 (2011): Issue 1 (June 2011)