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Biochemical and Biophysical Research Communications|August 16, 1990
Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathyP A Bolhuis, E M Bleeker-Wagemakers, N J Ponne, et al.
The New England Journal of Medicine|January 25, 1996
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastomaH Caron, P van Sluis, J de Kraker, et al.
Genomics|October 10, 1995
Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5T J Hulsebos, D J Gilbert, O Delattre, et al.
Annals of Surgical Oncology|September 21, 2013
Prognosis of solitary fibrous tumors: a multicenter studyWinan J van Houdt, Charlotte M A Westerveld, Joyce E P Vrijenhoek, et al.
Mutation Research|March 1, 1989
The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through IM van Duin, G Vredeveldt, L V Mayne, et al.
Human Molecular Genetics|April 1, 1995
Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplificationH Caron, M Peter, P van Sluis, et al.
Genomics|March 1, 1993
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family membersJ M Hoovers, E Redeker, F Speleman, et al.
Nature Genetics|June 1, 1993
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplificationH Caron, P van Sluis, M van Hoeve, et al.
Progress in Clinical and Biological Research|January 1, 1990
Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomesJ M Tager, S Brul, E A Wiemer, et al.
The Journal of Clinical Investigation|June 1, 1988
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysisS Brul, A Westerveld, A Strijland, et al.
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