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Bollettino Chimico Farmaceutico|April 7, 1998
[Formulation and stability of suspensions for preclinical study]S Burgalassi, G Perini, B Giannaccini, et al.Journal of Medical Genetics|March 1, 1997
A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivityR Tupler, G L Marseglia, M Stefanini, et al.Journal of Medical Genetics|May 1, 1996
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophyR Tupler, A Berardinelli, L Barbierato, et al.Journal of Medical Genetics|September 11, 1998
Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expressionR Tupler, L Barbierato, M Memmi, et al.Human Genetics|April 1, 1989
Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?O Zuffardi, A Caiulo, P Maraschio, et al.American Journal of Human Genetics|December 11, 2002
A locus for migraine without aura maps on chromosome 14q21.2-q22.3D Soragna, A Vettori, G Carraro, et al.Minerva Medica|January 7, 1976
[Ultrasonics in diagnosis of the upper abdomen]F Destro, P L Ceccarello, A Capozzi, et al.Ophthalmic Research|January 1, 1996
Effect of suleparoide on fibrinolysis in the anterior chamber of rabbitsA Lepri, U Benelli, P Chetoni, et al.Journal of Medical Genetics|January 1, 1992
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndromeR Tupler, L Bortotto, E M Bühler, et al.Pageof 7