Jolanda Gyftodimou

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

Lennart Iselius, J. Lindsten, Alain Aurias et al. · Human Genetics · 1983 · 189 citations

Human Migration, New Cases, Collaborative Study

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis

Voula Velissariou, Thalia Antoniadi, Jolanda Gyftodimou et al. · European Journal of Human Genetics · 2002 · 81 citations · Full text

Infertility, Developmental Biology, Cytogenetics +10

Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome

Michael Wang, Albert Schinzel, Dieter Kotzot et al. · American Journal of Medical Genetics · 1999 · 74 citations

Genetic Testing, Wbs Common Deletion, Genetic Disorder +14

Prevalence of GJB2 mutations in prelingual deafness in the Greek population

John R. Economides, Vasiliki Iliadou, Polyxeni Neou et al. · International Journal of Pediatric Otorhinolaryngology · 2002 · 63 citations

Mendelian Disorder, Greek Population, Genetic Disorder +8

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy

Mazin Β. Qumsiyeh, Syed K. Rafi, Catherine Sarri et al. · American Journal of Medical Genetics Part A · 2002 · 57 citations

Cytogenetics, Genetics, Pathology +17