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Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y-chromosome instability.
Patsalis PC, Skordis N, Sismani C, Kousoulidou L, Koumbaris G, Eftychi C, Stavrides G, Ioulianos A, Kitsiou-Tzeli S, Galla-Voumvouraki A, Kosmaidou Z, Hadjiathanasiou CG, McElreavey K. Patsalis PC, et al. Among authors: galla voumvouraki a. Am J Med Genet A. 2005 Jun 1;135(2):145-9. doi: 10.1002/ajmg.a.30712. Am J Med Genet A. 2005. PMID: 15880425
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB, et al. Karadima G, et al. Among authors: galla voumvouraki a. Eur J Hum Genet. 1998 Sep-Oct;6(5):432-8. doi: 10.1038/sj.ejhg.5200212. Eur J Hum Genet. 1998. PMID: 9801867
Partial disomy of Xp and the presence of SRY in a phenotypic female.
Bajalica S, Blennow E, Tşezou A, Galla-Voumvouraki A, Alevizaki M, Sinaniotis C, Kitsiou-Tzeli S. Bajalica S, et al. Among authors: galla voumvouraki a. J Med Genet. 1995 Dec;32(12):987-90. doi: 10.1136/jmg.32.12.987. J Med Genet. 1995. PMID: 8825932 Free PMC article.
Cytogenetic studies in children on long-term anticonvulsant therapy.
Kitsiou-Tzeli S, Galla-Voumvouraki A, Tsezou A, Kavazarakis E, Skardoutsou A, Koukoutsakis P, Sinamniotis C. Kitsiou-Tzeli S, et al. Among authors: galla voumvouraki a. Acta Paediatr. 1994 Jun;83(6):672-3. doi: 10.1111/j.1651-2227.1994.tb13110.x. Acta Paediatr. 1994. PMID: 7919770 No abstract available.