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Cytogenetics and Cell Genetics
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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 hybridization
G 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 sons
V 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 cells
G Calabrese, E Morizio, P Guanciali Franchi, et al.
Haematologica
|
November 7, 2000
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping
G Calabrese, D Fantasia, A Spadano, et al.
Genomics
|
November 1, 1994
Assignment of the beta-arrestin 1 gene (ARRB1) to human chromosome 11q13
G Calabrese, M Sallese, A Stornaiuolo, et al.
Cancer Genetics and Cytogenetics
|
October 15, 1993
Cytogenetic survey of benign prostate hyperplasia
G Calabrese, E Morizio, T Verna, et al.
Human Genetics
|
December 1, 1996
Molecular studies in three patients with isodicentric Y chromosome
L 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 female
G 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 crisis
L 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.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 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 hybridization
G 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 sons
V 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 cells
G Calabrese, E Morizio, P Guanciali Franchi, et al.
Haematologica
|
November 7, 2000
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping
G Calabrese, D Fantasia, A Spadano, et al.
Genomics
|
November 1, 1994
Assignment of the beta-arrestin 1 gene (ARRB1) to human chromosome 11q13
G Calabrese, M Sallese, A Stornaiuolo, et al.
Cancer Genetics and Cytogenetics
|
October 15, 1993
Cytogenetic survey of benign prostate hyperplasia
G Calabrese, E Morizio, T Verna, et al.
Human Genetics
|
December 1, 1996
Molecular studies in three patients with isodicentric Y chromosome
L 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 female
G 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 crisis
L 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.
Page
of 4