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Human Genetics|December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.Journal of Chemotherapy (Florence, Italy)|August 1, 1993
Lymphoblastoid interferon in advanced breast cancer: a phase II studyC Naso, C Simoni, L Merlini, et al.Human Mutation|April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. OnlineF Sangiuolo, A Botta, A Mesoraca, et al.Journal of Medical Genetics|November 1, 1994
Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patientsF Schiavon, M L Mostacciuolo, F Saad, et al.Muscle & Nerve|September 17, 1999
Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophyF Vitelli, M Villanova, A Malandrini, et al.Biochemical and Biophysical Research Communications|August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patientsM Gennarelli, M Lucarelli, F Capon, et al.Muscle & Nerve|May 22, 2001
Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophyP Sabatelli, G Lattanzi, A Ognibene, et al.Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.European Journal of Cancer (Oxford, England : 1990)|January 1, 1995
Long-term prognosis following macroscopic complete response at second-look laparotomy in advanced ovarian cancer patients treated with platinum-based chemotherapy. The Gruppo Oncologico Nord OvestS Chiara, R Lionetto, E Campora, et al.La Radiologia Medica|May 1, 1997
[Assessment of contrast enhancement in solitary pulmonary nodules studied with spiral computerized tomography. Preliminary results]M Tagliabue, I Macchi, L Merlini, et al.Pageof 18