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Human Genetics|June 19, 1979
Partial trisomy 16q resulting from maternal translocationP Balestrazzi, G Giovannelli, L Landucci Rubini, et al.Annales De Genetique|January 1, 1981
Evidence of gene dosage effect for HK 1 in the red cells of a patient with trisomy 10pter leads to p13B Dallapiccola, M Serena Lungarotti, M Magnani, et al.Journal of Medical Genetics|May 1, 1996
Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canalM C Digilio, B Marino, A Giannotti, et al.Journal of Medical Genetics|January 1, 1995
An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE)A Giannotti, M C Digilio, R Mingarelli, et al.Digestion|January 1, 1977
HLA and chronic active hepatitisM C Mazzilli, S Trabace, F D Raimondo, et al.Acta Dermato-Venereologica. Supplementum|January 1, 1994
Psoriatic arthritis: a clinical, radiological and genetic study of 58 Italian patientsS Trabace, S Cappellacci, P Ciccarone, et al.Journal of Medical Genetics|December 10, 1997
Conotruncal heart defect/microphthalmia syndrome: delineation of an autosomal recessive syndromeM C Digilio, B Marino, A Giannotti, et al.Giornale Italiano Di Cardiologia|April 1, 1991
[Trisomy 18 associated with atrioventricular canal]M C Digilio, B Marino, A Giannotti, et al.Rivista Di Neurologia|September 1, 1990
[Clinical study of two families with late-onset autosomal dominant spinal-cerebellar ataxia linked with HLA. Preliminary results]P Giunti, M Spadaro, M Frontali, et al.Italian Journal of Neurological Sciences|March 1, 1993
Target epitopes of myelin basic protein specific T cell lines in multiple sclerosisG Ristori, M Salvetti, C Buttinelli, et al.Pageof 38