Luitgard M. Neumann

Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

Martin Zenker, Thomas Aigner, Olaf Wendler et al. · Human Molecular Genetics · 2004 · 494 citations

Pierson Syndrome, Genetics, β2 Deficiency +18

Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome

Eva Klopocki, Harald Schulze, Gabriele Strauß et al. · The American Journal of Human Genetics · 2007 · 367 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

Marc Trimborn, Sandra Bell, Clive Felix et al. · The American Journal of Human Genetics · 2004 · 262 citations · Full text

Chromatin, Developmental Biology, Chromosome Condensation +6

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

Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition

Heidemarie Neitzel, Luitgard M. Neumann, Detlev Schindler et al. · The American Journal of Human Genetics · 2002 · 159 citations · Full text

Down Syndrome, Chromatin, Developmental Biology +11