A Galla-Voumvouraki

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism

Georgia Karadima, Merete Bugge, Peter Nicolaidis et al. · European Journal of Human Genetics · 1998 · 132 citations

Life Sciences, Genetics, Molecular Genetics +12

Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y‐chromosome instability

Philippos C. Patsalis, Nicos Skordis, Carolina Sismani et al. · American Journal of Medical Genetics Part A · 2005 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.

S. Kitsiou‐Tzeli, A Kolialexi, Helena Fryssira et al. · PubMed · 2005 · 41 citations

Life Sciences, Genetics, Molecular Genetics +15

Partial disomy of Xp and the presence of SRY in a phenotypic female.

Svetlana Bajalica, Elisabeth Blennow, Aspasia Tsezou et al. · Journal of Medical Genetics · 1995 · 12 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15