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Cancer Genetics and Cytogenetics
|
March 1, 1992
Cytogenetic survey of 80 patients with acute nonlymphocytic leukemia
G Palka, G Calabrese, G Fioritoni, et al.
Genes, Chromosomes & Cancer
|
May 1, 1991
Chromosome abnormalities in breast fibroadenomas
G Calabrese, C Di Virgilio, E Cianchetti, et al.
Haematologica
|
August 23, 2006
Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload
S Majore, F Milano, F Binni, et al.
Human Genetics
|
October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosis
G Calabrese, R Fischetto, L Stuppia, et al.
La Clinica Terapeutica
|
November 23, 2023
Omics sciences and precision medicine in lung cancer
C Micheletti, K Dhuli, K Donato, et al.
Haematologica
|
November 1, 1987
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL)
G Palka, G Fioritoni, M Lombardo, et al.
Muscle & Nerve
|
March 28, 2003
Dysmyelinating sensory-motor neuropathy in merosin-deficient congenital muscular dystrophy
A Di Muzio, M V De Angelis, P Di Fulvio, et al.
European Journal of Cell Biology
|
September 1, 1996
Multiple fluorescence and reflectance simultaneous detection by confocal microscopy of HaeIII digested DNA sequences
L M Neri, S Santi, C Cinti, et al.
Cellular Immunology
|
February 25, 1996
Human immunodeficiency virus type 1 tat protein modulates fibronectin expression in thymic epithelial cells and impairs in vitro thymocyte development
M Maroder, S Scarpa, I Screpanti, et al.
La Clinica Terapeutica
|
November 23, 2023
Omics sciences and precision medicine in sarcoma
G Bonetti, K Donato, K Dhuli, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 136) with videos related to
Sort By:
Page
of 14
Cancer Genetics and Cytogenetics
|
March 1, 1992
Cytogenetic survey of 80 patients with acute nonlymphocytic leukemia
G Palka, G Calabrese, G Fioritoni, et al.
Genes, Chromosomes & Cancer
|
May 1, 1991
Chromosome abnormalities in breast fibroadenomas
G Calabrese, C Di Virgilio, E Cianchetti, et al.
Haematologica
|
August 23, 2006
Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload
S Majore, F Milano, F Binni, et al.
Human Genetics
|
October 30, 1999
X/Y translocation in a family with Leri-Weill dyschondrosteosis
G Calabrese, R Fischetto, L Stuppia, et al.
La Clinica Terapeutica
|
November 23, 2023
Omics sciences and precision medicine in lung cancer
C Micheletti, K Dhuli, K Donato, et al.
Haematologica
|
November 1, 1987
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL)
G Palka, G Fioritoni, M Lombardo, et al.
Muscle & Nerve
|
March 28, 2003
Dysmyelinating sensory-motor neuropathy in merosin-deficient congenital muscular dystrophy
A Di Muzio, M V De Angelis, P Di Fulvio, et al.
European Journal of Cell Biology
|
September 1, 1996
Multiple fluorescence and reflectance simultaneous detection by confocal microscopy of HaeIII digested DNA sequences
L M Neri, S Santi, C Cinti, et al.
Cellular Immunology
|
February 25, 1996
Human immunodeficiency virus type 1 tat protein modulates fibronectin expression in thymic epithelial cells and impairs in vitro thymocyte development
M Maroder, S Scarpa, I Screpanti, et al.
La Clinica Terapeutica
|
November 23, 2023
Omics sciences and precision medicine in sarcoma
G Bonetti, K Donato, K Dhuli, et al.
Page
of 14