Vibeke Faurholt Pedersen

Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter

Marie Sogaard, Zeynep Tümer, Helle Hjalgrim et al. · BMC Medical Genetics · 2005 · 30 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Brothers with Chudley–McCullough syndrome: Sensorineural deafness, agenesis of the corpus callosum, and other structural brain abnormalities

Elsebet Østergaard, Vibeke Faurholt Pedersen, Elisabeth Skriver et al. · American Journal of Medical Genetics Part A · 2003 · 27 citations · Full text

Medicine, Neurology, Pediatrics +11

Clinical variability in three Danish patients with dihydropyrimidine dehydrogenase deficiency all homozygous for the same mutation

E. Christensen, I Cezanne, H Hørlyk et al. · Journal of Inherited Metabolic Disease · 1998 · 15 citations

Life Sciences, Genetics, Molecular Genetics +13

Winchester syndrome

G. Matthiesen, Vibeke Faurholt Pedersen, P. Helin et al. · International Orthopaedics · 2001 · 11 citations · Full text