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Cytogenetics and Cell Genetics|July 28, 2001
Characterization and chromosomal localization of five canine ATOX1 pseudogenesB van de Sluis, M S Nanji, M Breen, et al.
American Journal of Human Genetics|March 1, 1984
Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybridsP Wieacker, K E Davies, H J Cooke, et al.
Journal of Medical Genetics|October 1, 1990
Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the geneM H Breuning, F G Snijdewint, J G Dauwerse, et al.
Genomics|October 1, 1989
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinomaP Devilee, M van den Broek, N Kuipers-Dijkshoorn, et al.
European Journal of Clinical Investigation|November 26, 2003
Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch populationJ H van Tilburg, L A Sandkuijl, L Franke, et al.
American Journal of Human Genetics|June 13, 1998
Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphroditeJ C Giltay, T Brunt, F A Beemer, et al.
Cancer Genetics and Cytogenetics|March 24, 1999
Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell linesJ Kuipers, J W Vaandrager, D O Weghuis, et al.
Human Genetics|December 1, 1988
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursM Mannens, R M Slater, C Heyting, et al.
Human Genetics|January 1, 1985
The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24F Baas, H Bikker, A Geurts van Kessel, et al.
Human Genetics|August 1, 1986
Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridizationJ E Landegent, N Jansen in de Wal, Y M Fisser-Groen, et al.
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