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Annales De Genetique|June 1, 1975
Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.The New England Journal of Medicine|March 6, 1986
An inheritable anomaly of red-cell oxalate transport in "primary" calcium nephrolithiasis correctable with diureticsB Baggio, G Gambaro, F Marchini, et al.Pediatric Research|September 1, 1993
Respiratory mechanics in infants and young children before and after repair of left-to-right shuntsE Baraldi, M Filippone, O Milanesi, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1991
[Gastroesophageal reflux and infantile cerebral palsy: our experience and review of the literature]S Mazzoleni, P Drigo, L Da Dalt, et al.Human Heredity|May 1, 1993
Molecular characterization of 21-hydroxylase deficiency in 70 Italian familiesP Carrera, M Ferrari, F Beccaro, et al.American Journal of Medical Genetics|March 17, 1999
Methimazole embryopathy: delineation of the phenotypeM Clementi, E Di Gianantonio, E Pelo, et al.Brain & Development|March 1, 1992
Hyperthyroid-induced chorea in an adolescent girlG B Pozzan, P A Battistella, F Rigon, et al.European Journal of Pediatrics|December 10, 1997
Home oxygen therapy in infants with bronchopulmonary dysplasia: a prospective studyE Baraldi, S Carra, F Vencato, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1997
[Silent celiac disease: results of a study in secondary schools of Padua]G Guariso, M Plebani, R Signorini, et al.Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|March 10, 2007
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive geneM Clementi, E Di Gianantonio, L Fabris, et al.Pageof 18