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A Iolascon

Showing results (71-80 of 154) with videos related to

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Haematologica|September 1, 1994
Molecular heterogeneity of hereditary elliptocytosis in ItalyE Miraglia del Giudice, S Perrotta, E Sannino, et al.
International Journal of Laboratory Hematology|June 13, 2017
Diagnosis and molecular characterization of a novel α<sup>0</sup> -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemiaA Makis, I Georgiou, J Traeger-Synodinos, et al.
Minerva Cardioangiologica|February 18, 1999
[Genetic polymorphisms as thrombotic risk factors in patients with arterial and venous ischemic episodes]D De Lucia, G Maisto, R Marotta, et al.
La Pediatria|September 30, 1982
[Bart's hemoglobin in newborn infants of Campania]A Iolascon, B Nobili, L Pinto, et al.
The Journal of Pediatrics|February 7, 2001
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)S Perrotta, E M del Giudice, R Carbone, et al.
Journal of Medical Genetics|March 1, 1997
Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 geneA Bobba, A Iolascon, S Giannattasio, et al.
British Journal of Haematology|February 13, 2001
Clinical and molecular evaluation of non-dominant hereditary spherocytosisE Miraglia del Giudice, B Nobili, M Francese, et al.
Haematologica|March 26, 1999
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonatesA Iolascon, M F Faienza, S Perrotta, et al.
Genes, Chromosomes & Cancer|April 1, 1996
Analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, and CDKN2C) in childhood rhabdomyosarcomaA Iolascon, M F Faienza, B Coppola, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 1, 1993
p53 gene mutations in medulloblastoma. Immunohistochemistry, gel shift analysis, and sequencingM Badiali, A Iolascon, M Loda, et al.
Pageof 16

Showing results (71-80 of 154) with videos related to

Sort By:
Pageof 16
Haematologica|September 1, 1994
Molecular heterogeneity of hereditary elliptocytosis in ItalyE Miraglia del Giudice, S Perrotta, E Sannino, et al.
International Journal of Laboratory Hematology|June 13, 2017
Diagnosis and molecular characterization of a novel α<sup>0</sup> -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemiaA Makis, I Georgiou, J Traeger-Synodinos, et al.
Minerva Cardioangiologica|February 18, 1999
[Genetic polymorphisms as thrombotic risk factors in patients with arterial and venous ischemic episodes]D De Lucia, G Maisto, R Marotta, et al.
La Pediatria|September 30, 1982
[Bart's hemoglobin in newborn infants of Campania]A Iolascon, B Nobili, L Pinto, et al.
The Journal of Pediatrics|February 7, 2001
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)S Perrotta, E M del Giudice, R Carbone, et al.
Journal of Medical Genetics|March 1, 1997
Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 geneA Bobba, A Iolascon, S Giannattasio, et al.
British Journal of Haematology|February 13, 2001
Clinical and molecular evaluation of non-dominant hereditary spherocytosisE Miraglia del Giudice, B Nobili, M Francese, et al.
Haematologica|March 26, 1999
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonatesA Iolascon, M F Faienza, S Perrotta, et al.
Genes, Chromosomes & Cancer|April 1, 1996
Analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, and CDKN2C) in childhood rhabdomyosarcomaA Iolascon, M F Faienza, B Coppola, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 1, 1993
p53 gene mutations in medulloblastoma. Immunohistochemistry, gel shift analysis, and sequencingM Badiali, A Iolascon, M Loda, et al.
Pageof 16