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Molecular and Cellular Biology|June 1, 1990
Molecular cloning and biological characterization of the human excision repair gene ERCC-3G Weeda, R C van Ham, R Masurel, et al.
British Journal of Cancer|December 10, 1999
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2T J Hulsebos, N T Oskam, E H Bijleveld, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch familyM Mannens, E M Bleeker-Wagemakers, J Bliek, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC)S van Soest, S te Nijenhuis, L I van den Born, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|February 4, 2010
The dog as an animal model for DISH?H C Kranenburg, L A Westerveld, J J Verlaan, et al.
Human Genetics|March 1, 1996
No mutations found by RET mutation scanning in sporadic and hereditary neuroblastomaR M Hofstra, N C Cheng, C Hansen, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Nucleic Acids Research|September 1, 1996
Mutational analysis of the human nucleotide excision repair gene ERCC1A M Sijbers, P J van der Spek, H Odijk, et al.
Human Molecular Genetics|June 1, 1997
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblastsM Alders, M Hodges, A K Hadjantonakis, et al.
Human Genetics|December 1, 1986
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cellsF Arwert, H J Porck, M Fràter-Schröder, et al.
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