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Clinical Genetics|November 1, 1994
Patient with de novo 12p+ syndrome identified as dir dup (12) (p13) using subchromosomal painting libraries from somatic cell hybridsL Zelante, S Calvano, B Dallapiccola, et al.Annales De Genetique|January 1, 1992
Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patientsM G Obregon, R Mingarelli, M C Digilio, et al.Clinical Genetics|January 1, 1997
Two mosaic-YY males carrying asymmetric Y chromosomesL Zelante, B Dallapiccola, S Calvano, et al.Clinical Genetics|June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variantA Grifa, M R Piemontese, S Melchionda, et al.Nature Genetics|April 1, 1994
Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystineM J Calonge, P Gasparini, J Chillarón, et al.Cancer Genetics and Cytogenetics|May 1, 1987
Cytogenetics of Mendelian mutations associated with cancer pronenessB DallapiccolaHuman Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.Humangenetik|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 41