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Investigative Ophthalmology & Visual Science|April 1, 1983
X-linked incomplete achromatopsia with more than one class of functional conesV C Smith, J Pokorny, J W Delleman, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1990
Color matching and foveal densitometry in patients and carriers of an X-linked progressive cone dystrophyJ E Keunen, J A van Everdingen, L N Went, et al.Journal of the American Academy of Dermatology|November 1, 1990
Ocular melanoma in families with dysplastic nevus syndromeJ Vink, M B Crijns, C M Mooy, et al.Journal of Medical Genetics|April 1, 1991
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin geneM Losekoot, R Fodde, C L Harteveld, et al.British Journal of Cancer|October 1, 1981
Tumour spectrum in the FAMMM syndromeH T Lynch, R M Fusaro, J Pester, et al.Documenta Ophthalmologica. Advances in Ophthalmology|May 13, 2016
A family with sex linked optic atrophy : Ophthalmological and neurological aspectsH J Völker-Dieben, G H Van Lith, L N Went, et al.American Journal of Human Genetics|April 1, 1996
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystoniaD D De Vries, L N Went, G W Bruyn, et al.Human Genetics|January 1, 1984
Genetic linkage between erythrokeratodermia variabilis and Rh locusJ G van der Schroeff, L E Nijenhuis, P Meera Khan, et al.Human Genetics|January 1, 1984
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch familyF H Menko, O L Bijvoet, P Meera Khan, et al.Pageof 4