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American Journal of Medical Genetics|January 9, 2001
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotypeF Natacci, L Corrado, M Pierri, 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.
Acta Neurochirurgica|January 1, 1995
Intralesional administration of I-131 labelled monoclonal antibodies in the treatment of malignant gliomasA Arista, C Sturiale, P Riva, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|September 26, 2001
Heart rate variability in childhood obesityG Martini, P Riva, F Rabbia, 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.
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