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Journal of Clinical Pathology|July 29, 2005
An alternative protocol for DNA extraction from formalin fixed and paraffin wax embedded tissueR Coura, J C Prolla, L Meurer, et al.Jornal De Pediatria|March 1, 1996
[Inborn errors of metabolism: practical guidelines for clinical diagnosis in acutely ill children and infants]L B Jardim, P Ashton-ProllaAmerican Journal of Medical Genetics|June 27, 1997
Say syndrome: a new case with cystic renal dysplasia in discordant monozygotic twinsP Ashton-Prolla, T M FélixDiseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|February 13, 2003
Intestinal metaplasia in the distal esophagus and correlation with symptoms of gastroesophageal reflux diseaseJ Dietz, L Meurer, D R Maffazzoni, et al.The Journal of Clinical Investigation|March 17, 1999
Non-pseudogene-derived complex acid beta-glucosidase mutations causing mild type 1 and severe type 2 gaucher diseaseM E Grace, P Ashton-Prolla, G M Pastores, et al.Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1996
Maternal hyperphenylalaninaemia as a cause of microcephaly and mental retardationL B Jardim, R Palma-Dias, L C Silva, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|August 1, 2000
Fabry disease: twenty-two novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations in severely and mildly affected hemizygotes and heterozygotesP Ashton-Prolla, B Tong, J Shabbeer, et al.Acta Cytologica|July 31, 1998
Rapid rescreening of cervical smears for internal quality controlA R Diehl, J C ProllaJournal of Clinical Pathology|October 1, 1979
Clinical evaluation of eosinophils in the sputumV G Vieira, J C ProllaBoletin Chileno De Parasitologia|July 1, 1996
[Current prospects of specific treatment of Chagas' disease]J R CouraPageof 14