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G Gimelli

Showing results (41-50 of 64) with videos related to

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European Journal of Medical Genetics|November 7, 2020
17q23.3 de novo microdeletion involving only TANC2 gene: A new caseE Tassano, A Accogli, P Ronchetto, et al.
Human Genetics|March 1, 1986
First trimester fetal karyotyping: one thousand diagnosesG Simoni, G Gimelli, C Cuoco, et al.
Texas Heart Institute Journal|February 24, 2001
Endovascular treatment of a noninfected anastomotic juxtarenal aortic aneurysmG Melissano, C Di Mario, Y Tshomba, et al.
American Journal of Human Genetics|April 17, 1999
Transmission of a fully functional human neocentromere through three generationsC Tyler-Smith, G Gimelli, S Giglio, et al.
Oncology|May 1, 1994
Genotypic, phenotypic and biological characterization of a novel human lung adenocarcinoma cell line (LC 89)M Paganuzzi, P Marroni, A Pezzolo, et al.
The American Journal of Cardiology|December 1, 2001
Immediate and long-term clinical and angiographic results from Wiktor stent treatment for true bifurcation narrowingsA Anzuini, C Briguori, S Rosanio, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
Annali Di Ostetricia, Ginecologia, Medicina Perinatale|January 1, 1978
[Prenatal diagnosis by means of amniocentesis in the 2d trimester]E Porro, F Santi, G Gimelli, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1V Capra, M Severino, A Rossi, et al.
Human Genetics|January 1, 1982
Duplication of the short arm of chromosome 9. Analysis of five casesC Cuoco, G Gimelli, F Pasquali, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
European Journal of Medical Genetics|November 7, 2020
17q23.3 de novo microdeletion involving only TANC2 gene: A new caseE Tassano, A Accogli, P Ronchetto, et al.
Human Genetics|March 1, 1986
First trimester fetal karyotyping: one thousand diagnosesG Simoni, G Gimelli, C Cuoco, et al.
Texas Heart Institute Journal|February 24, 2001
Endovascular treatment of a noninfected anastomotic juxtarenal aortic aneurysmG Melissano, C Di Mario, Y Tshomba, et al.
American Journal of Human Genetics|April 17, 1999
Transmission of a fully functional human neocentromere through three generationsC Tyler-Smith, G Gimelli, S Giglio, et al.
Oncology|May 1, 1994
Genotypic, phenotypic and biological characterization of a novel human lung adenocarcinoma cell line (LC 89)M Paganuzzi, P Marroni, A Pezzolo, et al.
The American Journal of Cardiology|December 1, 2001
Immediate and long-term clinical and angiographic results from Wiktor stent treatment for true bifurcation narrowingsA Anzuini, C Briguori, S Rosanio, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
Annali Di Ostetricia, Ginecologia, Medicina Perinatale|January 1, 1978
[Prenatal diagnosis by means of amniocentesis in the 2d trimester]E Porro, F Santi, G Gimelli, et al.
American Journal of Medical Genetics. Part A|December 7, 2013
Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1V Capra, M Severino, A Rossi, et al.
Human Genetics|January 1, 1982
Duplication of the short arm of chromosome 9. Analysis of five casesC Cuoco, G Gimelli, F Pasquali, et al.
Pageof 7