Hubertus von Voß

Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients

Chayim Schell-Apacik, Kristina Wagner, Moritz Bihler et al. · American Journal of Medical Genetics Part A · 2008 · 197 citations · Full text

Corticobasal Degeneration, Genetics, Genetic Epidemiology +16

Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly

Sarah A. Shoichet, Stella‐Amrei Kunde, Petra Viertel et al. · Human Genetics · 2005 · 113 citations

Severe Mental Retardation, Mendelian Disorder, Brain Development +12

Association between life stress during pregnancy and infant crying in the first six months postpartum: A prospective longitudinal study

Harald Wurmser, Margarete Rieger, Caroline Domogalla et al. · Early Human Development · 2006 · 95 citations

Family Medicine, Perinatal Health, Prospective Longitudinal Study +14

Feeding disorders in ex-prematures: causes - response to therapy - long term outcome

Gereon Schädler, H Süss-Burghart, André Michael Toschke et al. · European Journal of Pediatrics · 2006 · 46 citations

Obesity, Nutrition, Infant Nutrition +12

A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum

Udo Koehler, Elke Holinski‐Feder, Birgit Ertl‐Wagner et al. · European Journal of Pediatrics · 2009 · 43 citations

Array Cgh, Mendelian Disorder, Genetic Disorder +10