M. Hagedorn-Greiwe

Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation

Jiong Tao, Hilde Van Esch, M. Hagedorn-Greiwe et al. · The American Journal of Human Genetics · 2004 · 322 citations · Full text

Developmental Anomaly, Severe Neurodevelopmental Retardation, Developmental Biology +11

Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation

Özge Altug Teber, Gabriele Gillessen‐Kaesbach, Sven Fischer et al. · European Journal of Human Genetics · 2004 · 178 citations · Full text

Developmental Anomaly, Molecular Diagnostic Techniques, Mendelian Disorder +9

Exclusion of Chromosome Regions 6p12 and 15q11, but Not Chromosome Region 7p11, in a German Family with Autosomal Dominant Congenital Nystagmus

Christine Klein, P. Vieregge, W. Heide et al. · Genomics · 1998 · 35 citations

Cytogenetics, Genetic Disorder, Genetics +8

Familial coexistence of primary antiphospholipid syndrome and factor VLeiden

M. Schütt, Harald Klüter, M. Hagedorn-Greiwe et al. · Lupus · 1998 · 26 citations

Histocompatibility, Genetics, Genetic Epidemiology +16