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Clinical Neuropharmacology|July 15, 2000
Beneficial effect of fluoxetine in a case of sporadic hyperekplexiaG Sechi, S Sotgiu, M P Valenti, et al.International Journal of Cancer|March 17, 1999
First cytogenetic study of a recurrent familial chordoma of the clivusL Dalprà, R Malgara, M Miozzo, et al.Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenomaD Bettio, D Giardino, N Rizzi, 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.Clinical Dysmorphology|August 24, 2000
Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1 biallelic expressionS Russo, M F Bedeschi, F Cogliati, et al.American Journal of Medical Genetics|October 26, 2000
Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian familyS Russo, F Cogliati, F Cavalleri, 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.Cancer Genetics and Cytogenetics|June 27, 2000
19p deletion in recurring leiomyosarcoma lesions from the same patientP Riva, L Dalprá, V Gualandri, et al.Clinical Genetics|December 15, 2015
Recognition of the Cornelia de Lange syndrome phenotype with facial dysmorphology novel analysisL Basel-Vanagaite, L Wolf, M Orin, et al.American Journal of Medical Genetics. Part A|August 25, 2010
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotypeD Concolino, G Roversi, G L Muzzi, et al.Pageof 11