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Human Genetics|September 22, 1977
Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213)B Dallapiccola, L Santoro, S Trabace, et al.American Journal of Medical Genetics|September 1, 1985
Osteoporosis-pseudoglioma syndrome: report of three affected sibs and an overviewM Frontali, C Stomeo, B DallapiccolaHuman Genetics|January 1, 1983
Mating between two balanced translocation carriers in two unrelated familiesB Dallapiccola, L Chessa, V Brinchi, et al.Prenatal Diagnosis|November 1, 1989
Prenatal diagnosis of adult polycystic kidney disease with DNA markers on chromosome 16 and the genetic heterogeneity problemG Novelli, M Frontali, D Baldini, et al.Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.Brain Research Bulletin|November 24, 2001
Spinocerebellar ataxia type 6: channelopathy or glutamine repeat disorder?M FrontaliCancer Genetics and Cytogenetics|May 1, 1987
Cytogenetics of Mendelian mutations associated with cancer pronenessB DallapiccolaHumangenetik|January 1, 1975
Observations on specific giemsa staining of the Y and on selective oil destaining of the chromosomesB Dallapiccola, N RicciAnnales De Genetique|January 1, 1988
Gene dosage studies regionally assign the phosphoserine phosphatase gene to 7p15.1 or 2G Novelli, B DallapiccolaHuman Genetics|April 27, 1979
Inactive normal X in a female leukaemic patient with an acquired X/autosome translocationB Dallapiccola, G AlimenaPageof 38