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Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Autosomal recessive mode of inheritance of a Coffin-Siris like syndromeE Bonioli, A Palmieri, A Bertola, et al.Journal of Computer Assisted Tomography|March 1, 1989
Leigh disease: value of CT in presymptomatic patients and variability of the lesions with timeA Taccone, M Di Rocco, P Fondelli, et al.American Journal of Diseases of Children (1960)|December 1, 1981
Karyotype-phenotype correlation in partial trisomy 13. Report of a case due to maternal translocationE Bonioli, M Crisalli, R Monteverde, et al.Journal De Genetique Humaine|June 1, 1978
[Trisomy of chromosome No. 10 in mosaic (author's transl)]M G Vianello, G Gemme, E Bonioli, et al.Minerva Pediatrica|November 1, 1990
[Sjögren's syndrome in childhood. Description of a clinical case]F Cottafava, D Cosso, M Faraci, et al.Fundamental & Clinical Pharmacology|January 1, 1991
Salicylic acid disposition in children with rheumatoid arthritisN Barzaghi, G Lamedica, G Gatti, et al.Minerva Pediatrica|July 1, 1993
[The Bartter-like syndrome in 2 twins]G Ruffa, M A Vigliarolo, P Sbolgi, et al.Vox Sanguinis|January 1, 1979
Chronic autoimmune neutropenia due to anti-NA1 antibodyM Valbonesi, A Campelli, M G Marazzi, et al.Minerva Pediatrica|June 1, 1992
[The Fanconi-Bickel syndrome: one more case]G Ruffa, M Ferrando, P Sbolgi, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1990
[Double-blind controlled comparison of placebo and paracetamol in patients with G-6-PD deficiency]F Cottafava, S Nieri, G Franzone, et al.Pageof 12