Bellinda van den Helm

Localization of the gene for Cowden disease to chromosome 10q22–23

Marcel Nelen, G.W. Padberg, E Peeters et al. · Nature Genetics · 1996 · 669 citations

Cowden Disease, Genetics, Pathogenesis +5

A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation

Helger G. Yntema, Bellinda van den Helm, J. Kissing et al. · Genomics · 1999 · 122 citations

Novel Ribosomal S6-kinase, Chromatin, Genetic Disorder +5

Localizaion of the gene for dominant cystoid macular dystrophy on chromosome 7p

Hannie Kremer, A. Pinckers, Bellinda van den Helm et al. · Human Molecular Genetics · 1994 · 113 citations

A Second Gene for Autosomal Dominant Möbius Syndrome Is Localized to Chromosome 10q, in a Dutch Family

H. T. F. M. Verzijl, Bellinda van den Helm, Bert Veldman et al. · The American Journal of Human Genetics · 1999 · 105 citations · Full text

Dutch Family, Mendelian Disorder, Cytogenetics +10

Familial X-linked mental retardation and isolated growth hormone deficiency: Clinical and molecular findings

Ben C.J. Hamel, Arie P.T. Smits, Barto J. Otten et al. · American Journal of Medical Genetics · 1996 · 69 citations