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| Nazaryan L, Stefanou EG, Hansen C, et al. (2014) The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. European Journal of Human Genetics : Ejhg. 22: 338-43 |
| Sismani C, Donoghue J, Alexandrou A, et al. (2013) A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13.2-q21.31 associated with multiple congenital abnormalities in a male fetus. Gene. 530: 138-42 |
| Velissariou V, Sismani C, Christopoulou S, et al. (2007) Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis. European Journal of Medical Genetics. 50: 291-300 |
| Velissariou V, Antoniadi T, Patsalis P, et al. (2001) Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis. Prenatal Diagnosis. 21: 484-7 |
| Patsalis PC, Sismani C, Hadjimarcou MI, et al. (1998) Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patients. Clinical Genetics. 53: 249-57 |
| Patsalis PC, Hadjimarcou MI, Velissariou V, et al. (1997) Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome. Clinical Genetics. 51: 184-90 |
| Velissariou V, Ashburner M. (1981) Cytogenetic and genetic mapping of a salivary gland secretion protein in Drosophila melanogaster. Chromosoma. 84: 173-85 |
| Velissariou V, Ashburner M. (1980) The secretory proteins of the larval salivary gland of Drosophila melanogaster: Cytogenetic correlation of a protein and a puff. Chromosoma. 77: 13-27 |