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Forabosco

Showing results (121-130 of 243) with videos related to

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Minerva Pediatrica|March 3, 1976
[Short arm chromosome 4 trisomy. Clinical aspects of a new syndrome]G Giovannelli, A Forabosco, L Rossi, et al.
The Anatomical Record|August 1, 1993
Morphometric study of the human ovary during compartmentalizationC Sforza, V F Ferrario, A De Pol, et al.
Biology of Reproduction|January 13, 2018
Lhx8 ablation leads to massive autophagy of mouse oocytes associated with DNA damageLaura D'Ignazio, Marc Michel, Melissa Beyer, et al.
Prenatal Diagnosis|April 9, 2008
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphaloceleAntonio Percesepe, Emma Bertucci, Paola Ferrari, et al.
JAMA Neurology|May 28, 2014
Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxiaConceição Bettencourt, Mina Ryten, Paola Forabosco, et al.
Developmental Biology|August 12, 1998
Timing of gene expression and oolemma localization of mouse alpha6 and beta1 integrin subunits during oogenesisM Zuccotti, P Giorgi Rossi, E Fiorillo, et al.
American Journal of Medical Genetics|July 23, 1998
Barber-Say Syndrome: report of a new caseL Mazzanti, R Bergamaschi, I Neri, et al.
Cytogenetics and Cell Genetics|January 1, 1995
A panel of subchromosomal painting libraries representing over 300 regions of the human genomeR Antonacci, R Marzella, P Finelli, et al.
Cytogenetics and Cell Genetics|July 7, 1999
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic geneF Gianfrancesco, T Esposito, A Ciccodicola, et al.
Italian Journal of Anatomy and Embryology = Archivio Italiano Di Anatomia Ed Embriologia|January 5, 2002
Morphological features and measurements in a human fetus with karyotype 69, XXX: comparison with fetuses of the same CRL, without chromosomal anomaliesR Bareggi, M A Sandrucci, A M Martelli, et al.
Pageof 25

Showing results (121-130 of 243) with videos related to

Sort By:
Pageof 25
Minerva Pediatrica|March 3, 1976
[Short arm chromosome 4 trisomy. Clinical aspects of a new syndrome]G Giovannelli, A Forabosco, L Rossi, et al.
The Anatomical Record|August 1, 1993
Morphometric study of the human ovary during compartmentalizationC Sforza, V F Ferrario, A De Pol, et al.
Biology of Reproduction|January 13, 2018
Lhx8 ablation leads to massive autophagy of mouse oocytes associated with DNA damageLaura D'Ignazio, Marc Michel, Melissa Beyer, et al.
Prenatal Diagnosis|April 9, 2008
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphaloceleAntonio Percesepe, Emma Bertucci, Paola Ferrari, et al.
JAMA Neurology|May 28, 2014
Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxiaConceição Bettencourt, Mina Ryten, Paola Forabosco, et al.
Developmental Biology|August 12, 1998
Timing of gene expression and oolemma localization of mouse alpha6 and beta1 integrin subunits during oogenesisM Zuccotti, P Giorgi Rossi, E Fiorillo, et al.
American Journal of Medical Genetics|July 23, 1998
Barber-Say Syndrome: report of a new caseL Mazzanti, R Bergamaschi, I Neri, et al.
Cytogenetics and Cell Genetics|January 1, 1995
A panel of subchromosomal painting libraries representing over 300 regions of the human genomeR Antonacci, R Marzella, P Finelli, et al.
Cytogenetics and Cell Genetics|July 7, 1999
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic geneF Gianfrancesco, T Esposito, A Ciccodicola, et al.
Italian Journal of Anatomy and Embryology = Archivio Italiano Di Anatomia Ed Embriologia|January 5, 2002
Morphological features and measurements in a human fetus with karyotype 69, XXX: comparison with fetuses of the same CRL, without chromosomal anomaliesR Bareggi, M A Sandrucci, A M Martelli, et al.
Pageof 25