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L Perroni

Showing results (41-50 of 49) with videos related to

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European Journal of Human Genetics : EJHG|April 26, 2000
FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brotherC Lo Nigro, F Faravelli, S Cavani, et al.
American Journal of Medical Genetics|July 12, 1996
Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: a study of 87 familiesL Perroni, M Grasso, A Argusti, et al.
Minerva Medica|July 28, 1970
[Radioisotope studies of thyroid hormone biosynthesis in immunological thyroiditis and in malignant tumors of the thyroid]O Ferrini, A Polleri, G L Perroni, et al.
American Journal of Medical Genetics|July 12, 1996
Prenatal diagnosis of 30 fetuses at risk for fragile X syndromeM Grasso, L Perroni, S Colella, et al.
American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
British Journal of Haematology|October 29, 1998
Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21qS Cavani, C Perfumo, A Argusti, et al.
American Journal of Medical Genetics|July 12, 1996
Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneityP Chiurazzi, M Genuardi, L Kozak, et al.
American Journal of Medical Genetics|July 9, 1999
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patientsM Grasso, F Faravelli, C Lo Nigro, et al.
Nature Genetics|January 4, 2001
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfyR S Wildin, F Ramsdell, J Peake, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
European Journal of Human Genetics : EJHG|April 26, 2000
FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brotherC Lo Nigro, F Faravelli, S Cavani, et al.
American Journal of Medical Genetics|July 12, 1996
Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: a study of 87 familiesL Perroni, M Grasso, A Argusti, et al.
Minerva Medica|July 28, 1970
[Radioisotope studies of thyroid hormone biosynthesis in immunological thyroiditis and in malignant tumors of the thyroid]O Ferrini, A Polleri, G L Perroni, et al.
American Journal of Medical Genetics|July 12, 1996
Prenatal diagnosis of 30 fetuses at risk for fragile X syndromeM Grasso, L Perroni, S Colella, et al.
American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
British Journal of Haematology|October 29, 1998
Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21qS Cavani, C Perfumo, A Argusti, et al.
American Journal of Medical Genetics|July 12, 1996
Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneityP Chiurazzi, M Genuardi, L Kozak, et al.
American Journal of Medical Genetics|July 9, 1999
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patientsM Grasso, F Faravelli, C Lo Nigro, et al.
Nature Genetics|January 4, 2001
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfyR S Wildin, F Ramsdell, J Peake, et al.
Pageof 5