Gerard van Noort

Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ14-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene

Hans R. Waterham, Janet Koster, P. A. W. Mooyer et al. · The American Journal of Human Genetics · 2003 · 214 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)

Claudio Bruno, O. P. van Diggelen, Denise Cassandrini et al. · Neurology · 2004 · 132 citations

Life Sciences, Genetics, Molecular Genetics +17

A Congenital Variant of Glycogenosis Type IV

Gerard van Noort, Wim Straks, Otto van Diggelen et al. · Fetal and Pediatric Pathology · 1993 · 42 citations

Life Sciences, Genetics, Pediatrics +12

Synchronous tumours of the unilateral parotid gland: rare or undetected?

Clark J. Zeebregts, W. J. B. Mastboom, Gerard van Noort et al. · Journal of Cranio-Maxillofacial Surgery · 2003 · 42 citations

Medicine, Oncology, Pathology +11

An important role for chromosome 17, band q25, in the histogenesis of alveolar soft part sarcoma

Jannie van Echten, Eva van den Berg, Joop van Baarlen et al. · Cancer Genetics and Cytogenetics · 1995 · 39 citations

Life Sciences, Genetics, Molecular Genetics +11