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Cytogenetics and Cell Genetics|January 1, 1978
BSu restriction of DNA from cases exhibiting sex-chromosome abnormalitiesJ Kinross, M Fraccaro, S Scappaticci, et al.Annales De Genetique|January 1, 1991
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detectionE Maserati, F Pasquali, O Zuffardi, et al.Human Genetics|March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomesP Maraschio, R Tupler, E Rossi, 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.Acta Anthropogenetica|January 1, 1983
H-Y antigen in human X-autosome translocationsA Mayerova, O Zuffardi, P Maraschio, et al.Human Genetics|August 1, 1987
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesisF Waibel, G Scherer, M Fraccaro, et al.Genomics|October 1, 1991
A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesisB Bardoni, O Zuffardi, S Guioli, et al.Human Genetics|October 1, 1986
A 45,X male with a Yp/18 translocationE Maserati, F Waibel, B Weber, et al.American Journal of Human Genetics|December 1, 1993
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1)M L Brandi, G Weber, A Svensson, et al.Human Genetics|January 1, 1983
Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainmentM Fraccaro, O Zuffardi, E Bühler, et al.Pageof 9