Balkan Journal of Medical Genetics

PRENATAL DIAGNOSIS OF A NEW CASE: DE NOVO BALANCED NON-ROBERTSONIAN TRANSLOCATION INVOLVING t(15;22)(p11.2;q11.2)
Atli Eİ, Gurkan H, Atli E, Tozkir H, Varol GF, İnan C
*Corresponding Author: Emine İkbal Atli, Ph.D., Department of Medical Genetics Faculty of Medicine Trakya University, Edirne, Turkey. Tel: +90-554-253-40-30. Fax: +90-284-223-33-14. Email: emine.ikbal@ gmail.com
page: 69

REFERENCES

1. Moorhead PS, Nowell PC, Mellman WJ, Battips DM, Hungerford DA. Chromosome preparations of leukocytes cultured from human peripheral blood. Exp Cell Res. 1960; 20(3): 613-616. 2. Peter PA. Prenatal diagnosis of chromosomal abnormalities through chorionic villus sampling and amniocentesis. In: Milunsky A, Milunsky JM, Editors. Benn Genetic Disorders and the Fetus Diagnosis, Prevention, and Treatment, 7th ed. Hoboken, NJ, USA: Wiley Blackwell; 2015: 178-266. 3. Mangelschots K, Van Roy B, Speleman F, Van Roy N, Gheuens J, Beuten J, et al. Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: Characterization by fluorescence in situ hybridization and DNA analysis. Hum Genet. 1992; 89(4): 407-413. 4. Rupa D, Neeraja K, Deepak C, Swarna M. A rare balanced nonrobertsonian translocation involving acrocentric chromosomes: Chromosome abnormality of t(13;15)(p11.2; q22.1). J Hum Reprod Sci. 2016; 9(2): 128-130. 5. Frikha R, Turki F, Daoud S, Kaabi O, Louati R, Trabelsi O, et al. A rare familial non Robertsonian translocation involving chromosomes 15 and 21 and failure of reproduction: Is there a correlation? (2809S). Presented at the 64th Annual Meeting of the American Society of Human Genetics, San Diego, CA, USA, October 19 2014. Am Soc Hum Genet. 2014; 95(3): 214-221. 6. Kayhan G, Ergün MA, Biri AA, Karaoğuz MY. A prenatal tertiary trisomy resulting from balanced maternal 8;9 translocation. J Turk Ger Gynecol Assoc. 2011; 12(3): 183-185. 7. Sheth F, Liehr T, Shah K, Sheth J. Prader-Willi syndrome – type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation. Mol Cytogenet. 2015; 8: 52.

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