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European Journal of Medical Genetics|August 23, 2016
Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndromeP Jiraanont, R J Hagerman, G Neri, et al.
American Journal of Medical Genetics|November 1, 1993
Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1M Genuardi, M G Pomponi, V Sammito, et al.
Journal of Medical Genetics|October 1, 1993
Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3L Kozák, P Chiurazzi, M Genuardi, et al.
Cancer Genetics and Cytogenetics|July 15, 1988
Long-term cytogenetic effects of antineoplastic treatment in relation to secondary leukemiaM Genuardi, M Zollino, A Serra, et al.
Leukemia Research|January 1, 1991
Chronic myelogenous leukemia in the course of chronic lymphocytic leukemia: evidence for an independent clonal originM Zollino, M Genuardi, P Tanci, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Assisted reproductive technology and congenital overgrowth: some speculations on a case of Pallister-Killian syndromeP Chiurazzi, J Bajer, E Tabolacci, et al.
American Journal of Medical Genetics|August 15, 1993
Costello syndrome: further clinical delineation, natural history, genetic definition, and nosologyG Zampino, P Mastroiacovo, R Ricci, et al.
Leukemia Research|October 1, 1995
Constitutional trisomy 8 and myelodysplasia: report of a case and review of the literatureM Zollino, M Genuardi, J Bajer, et al.
American Journal of Medical Genetics|March 9, 1999
"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotypeM Zollino, T J Wright, C Di Stefano, et al.
European Journal of Haematology|March 1, 1988
Partial duplication of chromosome 1q preceding the development of an L3 lymphoblastic leukemia with t(8;14), secondary to treatment for Hodgkin's diseaseM Zollino, M Genuardi, R De Santis, et al.
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