Christina Kelbova

De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5′ end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations

Ying Yue, R. Farcas, Gundula Thiel et al. · European Journal of Human Genetics · 2007 · 84 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +9

Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation

J. Seidel, Simone Schiller, Christina Kelbova et al. · Clinical Genetics · 2001 · 83 citations

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: Detailed molecular cytogenetic characterization and review of the literature

Marina Manvelyan, Mariluce Riegel, Mònica Santos et al. · International Journal of Molecular Medicine · 2008 · 53 citations · Full text

Genetic Testing, Fertility, Cytogenetics +20

New cytogenetically visible copy number variant in region 8q21.2

Marina Manvelyan, Friedrich W. Cremer, Jeannette Lancé et al. · Molecular Cytogenetics · 2011 · 20 citations · Full text

Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome

Andreas Dufke, J. Seidel, M. Schöning et al. · Cytogenetic and Genome Research · 2000 · 15 citations

Developmental Anomaly, Developmental Biology, Wolf-hirschhorn Syndrome +14