PARTIAL TRISOMY 9p(p22→pter) FROM A MATERNAL TRANSLOCATION 4q35 AND 9p22
Mahjoubi F1,2, Nasiri F1, Torabi R2
*Corresponding Author: Frouzandeh Mahjoubi, The Blood Transfusion Organization Research Center (IBTO), Hemmat Express Way, Next to Milad Tower, Tehran, Iran; P.O Box: 14665-1157; Tel.: +9821-8860-1501-30; Fax: +9821-8860-1555; E-mail: Frouz@nigeb.ac.ir
page: 61

REFERENCES

1. Orye EV, Verhaaren H, Van Egmond H, Devloo-Blancquaert A. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect. Clin Genet. 1975; 7(2): 134-143. 2. McDevitt MA, Condon M, Stamberg J, Karp JE, Mc- Diarmid M. Fluorescent in situ hybridization (FISH) in bone marrow and peripheral blood of leukemia patients: implications for occupational surveillance. Mutat Res. 2007; 629(1): 24-31. 3. Jelin AP, Perry H, Hogue J, Oberoi S, Cotter PD, Klein OD. Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization. J Craniofac Surg. 2010; 21(5): 1376- 1379. 4. Rossi NF, Gatto AR, Cola PC, Souza DH, Moretti-Ferreira D, Giacheti CM. Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report. Genet Mol Res. 2009; 8(3): 1133-1138. 5. Wang XR, Luo RL, Dai XH, Liu JY. Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation. Yi Chuan. 2007; 29(7): 813-816. 6. Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan M S, El Gammal M, El Ruby M, Mohamed AM. Phenotypic and cytogenetic spectrum of 9p trisomy. Genet Couns. 2007; 18(1): 29-48. 7. Liu Y-H, Wang J, Wang X-Z, Dai H, Xia J-H. A boy with 9p+ resulting from maternal t(4 9)translocation a case report. Journal of Medical Colleges of PLA. 2007; 22(4): 255-258. 8. Ricart J, Pareja IE. Trisomy 9p associated with self-injured behaviour and multiple intractable keloids. J Eur Acad Dermatol Venereol. 2006; 20(8): 1020-1021. 9. Kasakyan S, Lohmann L, Aboura A, Quimsiyeh M, Menezo Y, Tachdjian G, Benkhalifa M. De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH. Mol Cytogenet. 2008; 23(1): 27. 10. Chen CP, Shih JC. Association of partial trisomy 9p and the Dandy-Walker malformation. Am J Med Genet A. 2005; 132A(1): 111-112. 11. Panasiuk B, Danik J, Luriel W, Stasiewicz-Jarocka B, Lesniewicz R, Sawicka A, Kaluzewski B, Midro AT. Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2. Adv Med Sci. 2009; 54(2): 203-210. 12. Gripenberg UHK, Iivanainen M, Kivimaki T. Free trisomy 9P in elderly woman. Ann Genet. 1977; 20(1): 36-40. 13. Schnater JM, Schouten-van Meeteren AY, Heins YM, Aronson DC. Hepatoblastoma in a patient with a partial trisomy 9p syndrome: a case report. Cancer Genet Cytogenet. 2005; 156(1): 77-79. 14. Haddad BR, Lin AE, Wyandt H, Milunsky A. Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24). J Med Genet. 1996; 33(12): 1045-1047. 15. Munoz SR, Fernandez MH, Puente JLT, Manjon-Cabeza AA, Grondona FRL. Trisomy 9p. Report of two new cases. An Pediatr (Barc). 2004; 61(4): 336-339. 16. Littooij ASH, Sinke R, van Tintelen RJ, Giltay PJC. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up. Am J Med Genet. 2002; 109(2): 125-132. 17. Sigmund JF, Heinz-Erian H, Rhomberg P, Wegner K. Cri du chat-syndrome in combination with partial trisomy 9 p. Padiatr Padol. 1986; 21(1): 61-67. 18. Wilson GN, Raj A, Baker D. The phenotypic and cytogenetic spectrum of partial trisomy 9. Am J Med Genet. 1985; 20(2): 277-282. 19. Sandig KR, Mucke J, Veit H. Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome. Hum Genet. 1979; 52(2): 175-178. 20. Al Achkar W, Wafa A, Moassass A, Liehr T. Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl. Mol Cytogenet. 2010; 3: 18. 21. Ozer O, Derbent M, Sahin FI, Yilmaz Z. Two cases with partial trisomy 9: cytogenetic and clinical findings. Genet Couns. 2010; 21(2): 205-213. 22. Vazquez-Cardenas A, Vasquez-Velasquez AI, Barros- Nunez P, Mantilla-Capacho J, Rocchi M, Rivera H. Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges. J Appl Genet. 2007; 48(3): 261-268.



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