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Alberto Sensi

Showing results (1-10 of 17) with videos related to

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International Journal of Pediatric Otorhinolaryngology|February 2, 2010
Genetic syndromes involving hearingAlessandro Martini, Ferdinando Calzolari, Alberto Sensi
The Journal of Steroid Biochemistry and Molecular Biology|June 26, 2007
In vitro short-term test evaluation of catecholestrogens genotoxicityDamiano Rossi, Vincenzo Aiello, Laura Mazzoni, et al.
American Journal of Medical Genetics. Part A|September 12, 2006
Familial occurrence of multiple pterygium syndrome: expression in a heterozygote of the recessive form or variability of the dominant form?Paolo Prontera, Alberto Sensi, Luciano Merlo, et al.
Case Reports in Pediatrics|June 12, 2015
Hyperinsulinemic Hypoglycaemia in a Turner Syndrome with Ring (X)Michela Cappella, Vanna Graziani, Antonella Pragliola, et al.
American Journal of Medical Genetics. Part A|April 12, 2011
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutationsAlberto Sensi, Stefano Ceruti, Patrizia Trevisi, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotypeAlberto Sensi, Paolo Prontera, Barbara Buldrini, et al.
European Journal of Medical Genetics|December 28, 2005
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotypeAnna Baroncini, Francesca Rivieri, Antonella Capucci, et al.
Genes|September 28, 2021
MED12 Mutation in Two Families with X-Linked Ohdo SyndromeLuca Rocchetti, Eloisa Evangelista, Luigia De Falco, et al.
Prenatal Diagnosis|May 10, 2006
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosisPaolo Prontera, Barbara Buldrini, Vincenzo Aiello, et al.
Biochimica Et Biophysica Acta|August 8, 2012
Downregulation of A(1) and A(2B) adenosine receptors in human trisomy 21 mesenchymal cells from first-trimester chorionic villiStefania Gessi, Stefania Merighi, Angela Stefanelli, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
International Journal of Pediatric Otorhinolaryngology|February 2, 2010
Genetic syndromes involving hearingAlessandro Martini, Ferdinando Calzolari, Alberto Sensi
The Journal of Steroid Biochemistry and Molecular Biology|June 26, 2007
In vitro short-term test evaluation of catecholestrogens genotoxicityDamiano Rossi, Vincenzo Aiello, Laura Mazzoni, et al.
American Journal of Medical Genetics. Part A|September 12, 2006
Familial occurrence of multiple pterygium syndrome: expression in a heterozygote of the recessive form or variability of the dominant form?Paolo Prontera, Alberto Sensi, Luciano Merlo, et al.
Case Reports in Pediatrics|June 12, 2015
Hyperinsulinemic Hypoglycaemia in a Turner Syndrome with Ring (X)Michela Cappella, Vanna Graziani, Antonella Pragliola, et al.
American Journal of Medical Genetics. Part A|April 12, 2011
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutationsAlberto Sensi, Stefano Ceruti, Patrizia Trevisi, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotypeAlberto Sensi, Paolo Prontera, Barbara Buldrini, et al.
European Journal of Medical Genetics|December 28, 2005
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotypeAnna Baroncini, Francesca Rivieri, Antonella Capucci, et al.
Genes|September 28, 2021
MED12 Mutation in Two Families with X-Linked Ohdo SyndromeLuca Rocchetti, Eloisa Evangelista, Luigia De Falco, et al.
Prenatal Diagnosis|May 10, 2006
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosisPaolo Prontera, Barbara Buldrini, Vincenzo Aiello, et al.
Biochimica Et Biophysica Acta|August 8, 2012
Downregulation of A(1) and A(2B) adenosine receptors in human trisomy 21 mesenchymal cells from first-trimester chorionic villiStefania Gessi, Stefania Merighi, Angela Stefanelli, et al.
Pageof 2