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O Zuffardi

Showing results (21-30 of 159) with videos related to

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Annals of Human Genetics|March 1, 1996
Mitotic recombination among acrocentric chromosomes' short armsU Guissani, B Facchinetti, G Cassina, et al.
Clinical Genetics|June 11, 2009
Inverted duplications deletions: underdiagnosed rearrangements??O Zuffardi, M Bonaglia, R Ciccone, et al.
Human Genetics|January 1, 1982
Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocationH H Ropers, O Zuffardi, E Bianchi, et al.
EMBO Reports|March 27, 2001
Mapping of a human centromere onto the DNA by topoisomerase II cleavageG Floridia, A Zatterale, O Zuffardi, et al.
Journal of Medical Genetics|March 1, 1988
Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndromeP Maraschio, O Zuffardi, T Dalla Fior, et al.
Journal of Medical Genetics|September 1, 1990
Chromosome imbalance, normal phenotype, and imprintingL Bortotto, E Piovan, R Furlan, et al.
Human Genetics|December 15, 1976
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosisG Gimelli, E Porro, F Santi, et al.
Clinical Genetics|March 1, 1977
The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunctionF Bergamo, F Crosato, D Francesconi, et al.
Lancet (London, England)|April 24, 1971
Fluorescence and Y translocation in XX malesM Fraccaro, L Tiepolo, O Zuffardi, et al.
Chromosoma|January 1, 1971
Changes in the fluorescence patterns of translocated Y chromosome segments in Drosophila melanogasterO Zuffardi, L Tiepolo, S Dolfini, et al.
Pageof 16

Showing results (21-30 of 159) with videos related to

Sort By:
Pageof 16
Annals of Human Genetics|March 1, 1996
Mitotic recombination among acrocentric chromosomes' short armsU Guissani, B Facchinetti, G Cassina, et al.
Clinical Genetics|June 11, 2009
Inverted duplications deletions: underdiagnosed rearrangements??O Zuffardi, M Bonaglia, R Ciccone, et al.
Human Genetics|January 1, 1982
Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocationH H Ropers, O Zuffardi, E Bianchi, et al.
EMBO Reports|March 27, 2001
Mapping of a human centromere onto the DNA by topoisomerase II cleavageG Floridia, A Zatterale, O Zuffardi, et al.
Journal of Medical Genetics|March 1, 1988
Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndromeP Maraschio, O Zuffardi, T Dalla Fior, et al.
Journal of Medical Genetics|September 1, 1990
Chromosome imbalance, normal phenotype, and imprintingL Bortotto, E Piovan, R Furlan, et al.
Human Genetics|December 15, 1976
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosisG Gimelli, E Porro, F Santi, et al.
Clinical Genetics|March 1, 1977
The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunctionF Bergamo, F Crosato, D Francesconi, et al.
Lancet (London, England)|April 24, 1971
Fluorescence and Y translocation in XX malesM Fraccaro, L Tiepolo, O Zuffardi, et al.
Chromosoma|January 1, 1971
Changes in the fluorescence patterns of translocated Y chromosome segments in Drosophila melanogasterO Zuffardi, L Tiepolo, S Dolfini, et al.
Pageof 16