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F Gurrieri

Showing results (21-30 of 37) with videos related to

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American Journal of Medical Genetics|January 30, 1995
Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: further evidence for the existence of a limb defect gene in 6q21F Gurrieri, M Cammarata, R M Avarello, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
The Simpson-Golabi-Behmel syndrome: A clinical case and a detective storyF Gurrieri, M G Pomponi, R Pietrobono, et al.
American Journal of Medical Genetics|February 1, 1991
X-linked mental retardation with marfanoid habitus: first report of four Italian patientsF Lalatta, E Livini, A Selicorni, et al.
American Journal of Medical Genetics. Part A|April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehogLivia Garavelli, C Zanacca, G Caselli, et al.
Neurology|April 1, 1997
The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsyA Battaglia, F Gurrieri, E Bertini, et al.
Lung Cancer (Amsterdam, Netherlands)|May 1, 2025
Beyond environmental risk: Genetic insights into lung cancer susceptibility through whole exome analysisC Lintas, R Petti, G Colella, et al.
Journal of Global Antimicrobial Resistance|December 29, 2021
Genomic characterisation of Escherichia coli isolates co-producing NDM-5 and OXA-1 from hospitalised patients with invasive infectionsS Corbellini, E Scaltriti, G Piccinelli, et al.
Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.
The Journal of Biological Chemistry|June 15, 1987
Structural and functional analysis of a growth-regulated gene, the human calcyclinS Ferrari, B Calabretta, J K deRiel, et al.
Clinical Genetics|February 13, 2001
Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21D Tackels-Horne, A Toburen, E Sangiorgi, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|January 30, 1995
Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: further evidence for the existence of a limb defect gene in 6q21F Gurrieri, M Cammarata, R M Avarello, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
The Simpson-Golabi-Behmel syndrome: A clinical case and a detective storyF Gurrieri, M G Pomponi, R Pietrobono, et al.
American Journal of Medical Genetics|February 1, 1991
X-linked mental retardation with marfanoid habitus: first report of four Italian patientsF Lalatta, E Livini, A Selicorni, et al.
American Journal of Medical Genetics. Part A|April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehogLivia Garavelli, C Zanacca, G Caselli, et al.
Neurology|April 1, 1997
The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsyA Battaglia, F Gurrieri, E Bertini, et al.
Lung Cancer (Amsterdam, Netherlands)|May 1, 2025
Beyond environmental risk: Genetic insights into lung cancer susceptibility through whole exome analysisC Lintas, R Petti, G Colella, et al.
Journal of Global Antimicrobial Resistance|December 29, 2021
Genomic characterisation of Escherichia coli isolates co-producing NDM-5 and OXA-1 from hospitalised patients with invasive infectionsS Corbellini, E Scaltriti, G Piccinelli, et al.
Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.
The Journal of Biological Chemistry|June 15, 1987
Structural and functional analysis of a growth-regulated gene, the human calcyclinS Ferrari, B Calabretta, J K deRiel, et al.
Clinical Genetics|February 13, 2001
Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21D Tackels-Horne, A Toburen, E Sangiorgi, et al.
Pageof 4