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E Morizio

Showing results (1-10 of 33) with videos related to

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Cytogenetics and Cell Genetics|April 18, 2001
Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridizationG Calabrese, C Crescenzi, E Morizio, et al.
Journal of Medical Genetics|June 19, 2002
A new case of Yq microdeletion transmitted from a normal father to two infertile sonsV Gatta, L Stuppia, G Calabrese, et al.
American Journal of Medical Genetics|March 3, 1998
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cellsG Calabrese, E Morizio, P Guanciali Franchi, et al.
Haematologica|November 7, 2000
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotypingG Calabrese, D Fantasia, A Spadano, et al.
Genomics|November 1, 1994
Assignment of the beta-arrestin 1 gene (ARRB1) to human chromosome 11q13G Calabrese, M Sallese, A Stornaiuolo, et al.
Cancer Genetics and Cytogenetics|October 15, 1993
Cytogenetic survey of benign prostate hyperplasiaG Calabrese, E Morizio, T Verna, et al.
Human Genetics|December 1, 1996
Molecular studies in three patients with isodicentric Y chromosomeL Stuppia, G Calabrese, P G Franchi, et al.
Clinical Genetics|February 1, 1994
A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn femaleG Palka, G Calabrese, L Stuppia, et al.
Cancer Genetics and Cytogenetics|October 6, 1997
p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisisL Stuppia, G Calabrese, R Peila, et al.
American Journal of Medical Genetics|December 22, 1999
FISH analysis in detecting 9p duplication (p22p24)P Guanciali Franchi, G Calabrese, E Morizio, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Cytogenetics and Cell Genetics|April 18, 2001
Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridizationG Calabrese, C Crescenzi, E Morizio, et al.
Journal of Medical Genetics|June 19, 2002
A new case of Yq microdeletion transmitted from a normal father to two infertile sonsV Gatta, L Stuppia, G Calabrese, et al.
American Journal of Medical Genetics|March 3, 1998
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cellsG Calabrese, E Morizio, P Guanciali Franchi, et al.
Haematologica|November 7, 2000
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotypingG Calabrese, D Fantasia, A Spadano, et al.
Genomics|November 1, 1994
Assignment of the beta-arrestin 1 gene (ARRB1) to human chromosome 11q13G Calabrese, M Sallese, A Stornaiuolo, et al.
Cancer Genetics and Cytogenetics|October 15, 1993
Cytogenetic survey of benign prostate hyperplasiaG Calabrese, E Morizio, T Verna, et al.
Human Genetics|December 1, 1996
Molecular studies in three patients with isodicentric Y chromosomeL Stuppia, G Calabrese, P G Franchi, et al.
Clinical Genetics|February 1, 1994
A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn femaleG Palka, G Calabrese, L Stuppia, et al.
Cancer Genetics and Cytogenetics|October 6, 1997
p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisisL Stuppia, G Calabrese, R Peila, et al.
American Journal of Medical Genetics|December 22, 1999
FISH analysis in detecting 9p duplication (p22p24)P Guanciali Franchi, G Calabrese, E Morizio, et al.
Pageof 4