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Journal of Medical Genetics|April 1, 1985
First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 casesB Brambati, G Simoni, C Danesino, et al.Human Genetics|May 1, 1993
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to YqB Bardoni, G Floridia, S Guioli, et al.Oncogene|April 12, 2011
OTX1 expression in breast cancer is regulated by p53A Terrinoni, I S Pagani, I Zucchi, et al.Human Genetics|January 1, 1982
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 casesF Pasquali, P Bernasconi, R Casalone, et al.Nature Genetics|August 1, 1994
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversalB Bardoni, E Zanaria, S Guioli, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.Human Genetics|January 1, 1983
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesL Iselius, J Lindsten, A Aurias, et al.Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.Human Genetics|January 1, 1981
Sex-reversed XY females with campomelic dysplasia are H-Y negativeF D Bricarelli, M Fraccaro, J Lindsten, et al.Pageof 9