L. Govaerts

Infantile Refsum disease: an inherited peroxisomal disorder

Bwee Tien Poll‐The, J. M. Saudubray, H. Ogier et al. · European Journal of Pediatrics · 1987 · 131 citations

Infantile Refsum Disease, Inherited Metabolic Disease, Pediatrics +2

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1‐5q31.3 in ten unbalanced carriers

Yvonne Arens, J.J.M. Engelen, L. Govaerts et al. · American Journal of Medical Genetics Part A · 2004 · 88 citations

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome

Johanna M. van Hagen, Jos N. van der Geest, Ruben S. van der Giessen et al. · Neurobiology of Disease · 2006 · 85 citations · Full text

Neurodegenerative Diseases, Neuropsychology, Mendelian Disorder +10

Cerebro-hepato-renal syndrome of zellweger: Clinical symptoms and relevant laboratory findings in 16 patients

L. Govaerts, L.A.H. Monnens, W. H. H. Tegelaers et al. · European Journal of Pediatrics · 1982 · 65 citations

Urology, Clinical Symptoms, Hepatology +8

A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus

Reinhard Oldenburg, M. F. van Dooren, Bianca de Graaf et al. · Human Reproduction · 2008 · 52 citations · Full text