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Cancer Genetics and Cytogenetics|April 12, 2001
Multicolor FISH in chronic lymphocytic leukemia. An interphase study of patients with early-onset diseaseL Doneda, P Castorina, A Tedeschi, et al.
Human Genetics|December 1, 1996
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndromeP Riva, P Castorina, S Manoukian, et al.
Cancer Genetics and Cytogenetics|May 17, 2000
Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvementA Beghini, C B Ripamonti, P Castorina, et al.
American Journal of Human Genetics|January 13, 2000
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probesP Riva, L Corrado, F Natacci, et al.
Hearing Research|January 11, 2015
Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosisS Lenarduzzi, D Vozzi, A Morgan, et al.
International Journal of Cancer|July 29, 1998
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndromeM Miozzo, P Castorina, P Riva, et al.
Clinical Genetics|September 17, 2013
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of casesC Fallerini, L Dosa, R Tita, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
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