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G Calabrese

Showing results (211-220 of 238) with videos related to

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Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane geneG Calabrese, L Stuppia, E Morizio, et al.
Journal of Endocrinological Investigation|March 24, 2006
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase gamma gene is not associated with oligozoospermiaA Brusco, C Michielotto, V Gatta, et al.
Applied and Environmental Microbiology|December 1, 1992
Gene probe analysis of soil microbial populations selected by amendment with 2,4-dichlorophenoxyacetic acidW E Holben, B M Schroeter, V G Calabrese, et al.
Cancer Genetics and Cytogenetics|February 1, 1991
Cytogenetic survey of 31 patients treated with bone marrow transplantation for acute nonlymphocytic and acute lymphoblastic leukemiasG Palka, G Calabrese, G Di Girolamo, et al.
Minerva Ginecologica|July 1, 1990
[Cytogenetic study of 201 subjects with altered reproductive fitness]G D Palka, P G Bianchi, G Calabrese, et al.
Journal of Medical Genetics|October 3, 1999
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X maleL Stuppia, G Calabrese, P Borrelli, et al.
Radiology|April 1, 1992
Alterations in brain phosphorus metabolite concentrations associated with areas of high signal intensity in white matter at MR imagingD Sappey-Marinier, R F Deicken, G Fein, et al.
The Review of Scientific Instruments|July 7, 2023
Experimental characterization of gaseous ion beams produced with the advanced ion source for hadrontherapy (AISHa) at 18 GHzG Castro, O Leonardi, F Chines, et al.
The Review of Scientific Instruments|November 30, 2019
Experimental characterization of the AISHa ion sourceL Celona, G Calabrese, G Castro, et al.
Pageof 24

Showing results (211-220 of 238) with videos related to

Sort By:
Pageof 24
Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane geneG Calabrese, L Stuppia, E Morizio, et al.
Journal of Endocrinological Investigation|March 24, 2006
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase gamma gene is not associated with oligozoospermiaA Brusco, C Michielotto, V Gatta, et al.
Applied and Environmental Microbiology|December 1, 1992
Gene probe analysis of soil microbial populations selected by amendment with 2,4-dichlorophenoxyacetic acidW E Holben, B M Schroeter, V G Calabrese, et al.
Cancer Genetics and Cytogenetics|February 1, 1991
Cytogenetic survey of 31 patients treated with bone marrow transplantation for acute nonlymphocytic and acute lymphoblastic leukemiasG Palka, G Calabrese, G Di Girolamo, et al.
Minerva Ginecologica|July 1, 1990
[Cytogenetic study of 201 subjects with altered reproductive fitness]G D Palka, P G Bianchi, G Calabrese, et al.
Journal of Medical Genetics|October 3, 1999
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X maleL Stuppia, G Calabrese, P Borrelli, et al.
Radiology|April 1, 1992
Alterations in brain phosphorus metabolite concentrations associated with areas of high signal intensity in white matter at MR imagingD Sappey-Marinier, R F Deicken, G Fein, et al.
The Review of Scientific Instruments|July 7, 2023
Experimental characterization of gaseous ion beams produced with the advanced ion source for hadrontherapy (AISHa) at 18 GHzG Castro, O Leonardi, F Chines, et al.
The Review of Scientific Instruments|November 30, 2019
Experimental characterization of the AISHa ion sourceL Celona, G Calabrese, G Castro, et al.
Pageof 24