MOLECULAR CYTOGENETIC CHARACTERIZATION OF AN inv(Y)(p11.2q11.221~q11.222) IN A SYRIAN FAMILY
Al-Achkar W1,*, Wafa A1, Al-Ablog A1, Moassass F1, Liehr T2
*Corresponding Author: Professor Walid Al-Aachkar, Department of Molecular Biology and Biotechnology, Division of Human Genetics, Atomic Energy Commission of Syria, P.O. Box 6091, Damascus, Syria; Tel.: +963- 11-213-2580; Fax: +963-11-611-2289; E-mail: ascientific@aec.org.sy
page: 73

REFERENCES

1. Bernstein R, Wadee A, Rosendorff J, Wessels A, Jenkins T. Inverted Y chromosome polymorphism in the Gujerati Muslim Indian population of South Africa. Hum Genet. 1986; 74(3): 223-229. 2. Tóth A, Gaál M, László J. Familial pericentric inversion of the Y chromosome. Ann Genet. 1984; 27(1): 60-61. 3. Motos Guirao MA. Pericentric inversion of the human Y chromosome. An Esp Pediatr. 1989; 31(6): 583-587. 4. Shapiro LR, Pettersen RO, Wilmot PL, Warburton D, Benn PA, Hsu LY. Pericentric inversion of the Y chromosome and prenatal diagnosis. Prenat Diagn. 1984; 4(6): 463-465. 5. Schmid M. Variations of content and structure of the mammalian Y chromosome, in Sandberg AA, Ed. The Y Chromosome, Part A, Basic Characteristics of the Y Chromosome. New York: Alan R. Liss. 1985: 373-401. 6. Luo YQ, Qian YL, Lu HM, Xu CM, Jin F. Sperm-fluorescence in situ hybridization analysis in patients with pericentric inversions of Y chromosome. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009; 26(1): 54-56. 7. Marchina E, Imperadori L, Speziani M, Omodei U, Tombesi S, Barlati S. Chromosome abnormalities and Yq microdeletions in infertile italian couples referred for assisted reproductive technique. Sex Dev. 2007; 1(6): 347-352. 8. Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez L, Martínez Guardia N, et al. Small supernumerary marker chromosomes–progress towards a genotype-phenotype correlation. Cytogenet Genome Res. 2006; 112(1-2): 23-34. 9. Tomomasa H, Adachi Y, Iwabuchi M, Oshio S, Umeda T, Iino Y, et al. Pericentric inversion of the Y chromosome of infertile male. Arch Androl. 2000; 45(3): 181-185. 10. Causio F, Canale D, Schonauer LM, Fischetto R, Leonetti T, Archidiacono N. Breakpoint of a Y chromosome pericentric inversion in the DAZ gene area. A case report. J Reprod Med. 2000; 45(7): 591-594. 11. Shaffer L, Slovak M, Cambell L, Eds. ISCN (2009): An International System for Human Cytogenetic Nomenclature. Basel: S. Karger, 2009. 12. Al-Achkar W, Wafa A, Liehr T, Klein E, Moassass F. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. Mol Med Report. 2012; 6(2): 293-296. 13. Jacobs PA, Hassold TJ. Chromosome abnormalities: origin and etiology in abortions and livebirths. In: Vogel F, Sperling K, Eds. Human Genetics. Berlin: Springer. 1987: 233-244. 14. Hsu LY, Benn PA, Tannenbaum HL, Perlis TE, Carlson AD. Chromosomal polymorphisms of 1, 9, 16, and Y in 4 major ethnic groups: a large prenatal study. Am J Med Genet. 1987; 26(1): 95-101. 15. Mahajan S, Kaur A, Singh JR. Cytogenetic investigations in mentally challenged individuals. Int J Hum Genet. 2011; 11(2): 93-98. 16. Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L, Brown LG, et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature. 2003; 423(6942): 825-837. 17. Knebel S, Pasantes JJ, Thi DA, Schaller F, Schempp W. Heterogeneity of pericentric inversions of the human y chromosome. Cytogenet Genome Res. 2011; 132(4): 219-226.



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