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Cytogenetics and Cell Genetics|January 1, 1997
Identification of positional candidates for neurological disorders on chromsome 13q14-->q22H G Nothwang, J Wirth, B Brandl, et al.Human Genetics|January 1, 1980
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223L Tiepolo, O Zuffardi, M Fraccaro, et al.Clinical Genetics|September 14, 2007
Cytogenetically invisible microdeletions involving PITX2 in Rieger syndromeE Engenheiro, J Saraiva, I Carreira, et al.Human Genetics|September 1, 1988
Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosomeN Knoers, H van der Heyden, B A van Oost, et al.Nature Genetics|October 31, 2001
MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradationA Trockenbacher, V Suckow, J Foerster, et al.Cytogenetics and Cell Genetics|January 1, 1986
Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosomeT Hulsebos, B Wieringa, R Hochstenbach, et al.Human Genetics|May 1, 1993
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11qE C Mariman, S E van Beersum, C W Cremers, et al.Genomics|April 1, 1989
Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidusN Knoers, H van der Heyden, B A van Oost, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 9, 1999
Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?K Stout, S van der Maarel, R R Frants, et al.Acta Anthropogenetica|January 1, 1983
H-Y antigen in human X-autosome translocationsA Mayerova, O Zuffardi, P Maraschio, et al.Pageof 21