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E Morizio

Showing results (21-30 of 33) with videos related to

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Journal of Medical Genetics|October 1, 1994
A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasiaG Calabrese, P G Franchi, L Stuppia, et al.
Cytogenetic and Genome Research|November 17, 2011
A new case of pure partial 7q duplicationM Alfonsi, C Palka, E Morizio, et al.
Cancer Genetics and Cytogenetics|October 1, 1996
Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysisG Calabrese, T Min, L Stuppia, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kbG Calabrese, L Telvi, F Capodiferro, et al.
Genomics|June 13, 2001
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) geneL Stuppia, V Gatta, I Fogh, et al.
Human Genetics|July 8, 1998
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11L Stuppia, V Gatta, G Calabrese, et al.
Cancer Genetics and Cytogenetics|December 1, 1994
Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysisG Calabrese, L Stuppia, P G Franchi, 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 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.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown causeE Morizio, L Stuppia, V Gatta, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|October 1, 1994
A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasiaG Calabrese, P G Franchi, L Stuppia, et al.
Cytogenetic and Genome Research|November 17, 2011
A new case of pure partial 7q duplicationM Alfonsi, C Palka, E Morizio, et al.
Cancer Genetics and Cytogenetics|October 1, 1996
Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysisG Calabrese, T Min, L Stuppia, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kbG Calabrese, L Telvi, F Capodiferro, et al.
Genomics|June 13, 2001
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) geneL Stuppia, V Gatta, I Fogh, et al.
Human Genetics|July 8, 1998
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11L Stuppia, V Gatta, G Calabrese, et al.
Cancer Genetics and Cytogenetics|December 1, 1994
Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysisG Calabrese, L Stuppia, P G Franchi, 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 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.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown causeE Morizio, L Stuppia, V Gatta, et al.
Pageof 4