REFERENCES
- Cyrus C, Kaur H, Koshy T, A de novo reciprocal t(2;18) translocation with regular trisomy 21. Genet Test 11:459–462, 2007.
- Butomo IV, Mashkova MV. Double autosomal aberration: trisomy 21 and familial reciprocal translocation t(10;12)(p14;q21). Tsitologiia 19:1291–1296, 1977.
- Stefanova M, Atanassov D, Krastev T, Zimmermann–Laband syndrome associated with a balanced reciprocal translocation t(3;8) (p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions. Am J Med Genet A 117:289–294, 2003.
- Debrus S, de Meeus A, Jean MK, Bouvagnet P. Genetics of hereditary cardiopathies. Arch Mal Coeur Vaiss 89:619–627, 1996.
- Hesson LB, Cooper WN, Latif F. Evaluation of the 3p21.3 tumour-suppressor gene cluster. Oncogene 26:7283–7301, 2007.
- Ghoussaini M, Song H, Koessler T, UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons’ Section of Oncology; UK ProtecT Study Collaborators. Multiple loci with different cancer specificities within the 8q24 gene desert. J Natl Cancer Inst 100:962–966, 2008.
- Verheij JB, de Munnik SA, Dijkhuizen T, An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions. Eur J Med Genet 52:353–357, 2009.
- Karacay S, Saygun I, Tunca Y, Clinical and intraoral findings of a patient with tricho–rhino–phalangeal syndrome type I. J Indian Soc Pedod Prev Dent 25:43–45, 2007.