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M C Rosatelli

Showing results (1-10 of 41) with videos related to

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Bailliere'S Clinical Haematology|March 1, 1993
Screening and prenatal diagnosis of the haemoglobinopathiesA Cao, M C Rosatelli
Ciba Foundation Symposium|January 1, 1996
Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experienceA Cao, M C Rosatelli, R Galanello
Bailliere'S Clinical Haematology|June 29, 2000
Prenatal diagnosis and screening of the haemoglobinopathiesA Cao, R Galanello, M C Rosatelli
Blood Reviews|March 1, 1994
Genotype-phenotype correlations in beta-thalassemiasA Cao, R Galanello, M C Rosatelli
Current Opinion in Genetics & Development|June 1, 1991
Population-based genetic screeningA Cao, M C Rosatelli, R Galanello
Journal of Medical Genetics|February 24, 2001
Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) geneA Iolascon, A Meloni, B Coppola, et al.
Human Mutation|January 1, 1996
New frameshift mutation in the DAX-1 gene in a patient with X-linked adrenal hypoplasia and hypogonadotropic hypogonadismA Meloni, A Meloni, A Cao, et al.
Prenatal Diagnosis|September 1, 1987
Chorionic villus sampling and acceptance rate of prenatal diagnosisA Cao, P Cossu, G Monni, et al.
JAMA|October 23, 1997
Molecular diagnosis and carrier screening for beta thalassemiaA Cao, L Saba, R Galanello, et al.
Genetics and Molecular Research : GMR|December 16, 2014
Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patientsS Lenarduzzi, M Morgutti, S Crovella, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Bailliere'S Clinical Haematology|March 1, 1993
Screening and prenatal diagnosis of the haemoglobinopathiesA Cao, M C Rosatelli
Ciba Foundation Symposium|January 1, 1996
Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experienceA Cao, M C Rosatelli, R Galanello
Bailliere'S Clinical Haematology|June 29, 2000
Prenatal diagnosis and screening of the haemoglobinopathiesA Cao, R Galanello, M C Rosatelli
Blood Reviews|March 1, 1994
Genotype-phenotype correlations in beta-thalassemiasA Cao, R Galanello, M C Rosatelli
Current Opinion in Genetics & Development|June 1, 1991
Population-based genetic screeningA Cao, M C Rosatelli, R Galanello
Journal of Medical Genetics|February 24, 2001
Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) geneA Iolascon, A Meloni, B Coppola, et al.
Human Mutation|January 1, 1996
New frameshift mutation in the DAX-1 gene in a patient with X-linked adrenal hypoplasia and hypogonadotropic hypogonadismA Meloni, A Meloni, A Cao, et al.
Prenatal Diagnosis|September 1, 1987
Chorionic villus sampling and acceptance rate of prenatal diagnosisA Cao, P Cossu, G Monni, et al.
JAMA|October 23, 1997
Molecular diagnosis and carrier screening for beta thalassemiaA Cao, L Saba, R Galanello, et al.
Genetics and Molecular Research : GMR|December 16, 2014
Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patientsS Lenarduzzi, M Morgutti, S Crovella, et al.
Pageof 5