Ulrike Kordaß

Duplications of <i>BHLHA9</i> are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion

Eva Klopocki, Silke B. Lohan, Sandra C. Doelken et al. · Journal of Medical Genetics · 2011 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Deleterious de novo variants of X‐linked <i>ZC4H2</i> in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita

Suzanna G.M. Frints, Friederike Hennig, Roberto Colombo et al. · Human Mutation · 2019 · 47 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

Jasmin Beygo, Alma Küchler, Gabriele Gillessen‐Kaesbach et al. · European Journal of Human Genetics · 2017 · 45 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Two cases with severe lethal course of Costello syndrome associated with HRAS p.G12C and p.G12D

Sybille Lorenz, Christine Petersen, Ulrike Kordaß et al. · European Journal of Medical Genetics · 2012 · 31 citations

Medicine, Pathology, Molecular Pathology +1

Segmental maternal uniparental disomy 7q associated with <i>DLK1/GTL2</i> (14q32) hypomethylation

Matthias Begemann, Sabrina Spengler, Ulrike Kordaß et al. · American Journal of Medical Genetics Part A · 2012 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17