Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype
Zechner, U, Kohlschmidt, N, Rittner, G, Damatova, N, Beyer, V, Haaf, T, Bartsch, O
Published in Clinical genetics (01.03.2009)
Published in Clinical genetics (01.03.2009)
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Journal Article
Haploinsufficiency of 16.4 Mb from Chromosome 22pter-q11.21 in a Girl with Unilateral Conductive Hearing Loss
Damatova, N., Beyer, V., Galetzka, D., Schneider, E., Napiontek, U., Keilmann, A., Zechner, U., Bartsch, O., Haaf, T.
Published in Cytogenetic and genome research (01.01.2009)
Published in Cytogenetic and genome research (01.01.2009)
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Journal Article