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G Novelli

Showing results (171-180 of 330) with videos related to

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Cancer Gene Therapy|January 6, 2021
LOX-1 and cancer: an indissoluble liaisonM Murdocca, C De Masi, S Pucci, et al.
Human Genetics|April 1, 1996
Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridizationG Calabrese, R Mingarelli, P Francalanci, et al.
Prenatal Diagnosis|August 1, 1996
Ultrasound and molecular mid-trimester prenatal diagnosis of de novo achondroplasiaA Mesoraca, G Pilu, A Perolo, et al.
Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.
Journal of Medical Microbiology|September 1, 1996
Correlation of SfiI macrorestriction endonuclease fingerprint analysis of Candida parapsilosis isolates with source of isolationE Pontieri, L Gregori, M Gennarelli, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.
European Journal of Medical Genetics|May 6, 2006
Identification of a novel mutation in the SRY gene in a 46, XY female patientL Baghernajad Salehi, O Scarciolla, G Frajese Vanni, et al.
Prenatal Diagnosis|June 11, 1998
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markersI Torrente, M Mangino, A De Luca, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.
Pageof 33

Showing results (171-180 of 330) with videos related to

Sort By:
Pageof 33
Cancer Gene Therapy|January 6, 2021
LOX-1 and cancer: an indissoluble liaisonM Murdocca, C De Masi, S Pucci, et al.
Human Genetics|April 1, 1996
Diagnosis of DiGeorge syndrome in nuclei released from archival autoptic heart specimens using fluorescence in situ hybridizationG Calabrese, R Mingarelli, P Francalanci, et al.
Prenatal Diagnosis|August 1, 1996
Ultrasound and molecular mid-trimester prenatal diagnosis of de novo achondroplasiaA Mesoraca, G Pilu, A Perolo, et al.
Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.
Journal of Medical Microbiology|September 1, 1996
Correlation of SfiI macrorestriction endonuclease fingerprint analysis of Candida parapsilosis isolates with source of isolationE Pontieri, L Gregori, M Gennarelli, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.
European Journal of Medical Genetics|May 6, 2006
Identification of a novel mutation in the SRY gene in a 46, XY female patientL Baghernajad Salehi, O Scarciolla, G Frajese Vanni, et al.
Prenatal Diagnosis|June 11, 1998
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markersI Torrente, M Mangino, A De Luca, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.
Pageof 33