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Laura Bernardini

Showing results (11-20 of 157) with videos related to

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European Journal of Medical Genetics|July 5, 2015
Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndromeM Cristina Digilio, Paolo Versacci, Laura Bernardini, et al.
Journal of Pediatric Hematology/Oncology|July 9, 2003
Medulloblastoma as a secondary malignancy after radiotherapy-free treatment for acute lymphoblastic leukemiaAmalia Schiavetti, Anna Clerico, Maria Debora De Pasquale, et al.
Prenatal Diagnosis|May 29, 2013
Interstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosisAnna Capalbo, Lorenzo Sinibaldi, Laura Bernardini, et al.
Future Oncology (London, England)|May 6, 2024
Dabrafenib-trametinib in BRAF V600-mutated non-small-cell lung cancer: a single center real world experienceAndrea Sbrana, Sabrina Cappelli, Iacopo Petrini, et al.
Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Duplication 18q21.31-q22.2Caterina Ceccarini, Lorenzo Sinibaldi, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
TBX2 gene duplication associated with complex heart defect and skeletal malformationsFrancesca Clementina Radio, Laura Bernardini, Sara Loddo, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
X chromosome monosomy restricted to the left ventricle is not a major cause of isolated hypoplastic left heartLaura Bernardini, Maria Grazia Giuffrida, Paola Francalanci, et al.
European Journal of Medical Genetics|August 14, 2019
A novel mosaic 1q32.1 microduplication identified through Chromosome Microarray Analysis: narrowing the smallest critical region including KDM5B gene found associated with neurodevelopmetal disordersGianmaria Miolo, Maria Grazia Giuffrida, Giuseppe Corona, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 19, 2022
Critical prenatal diagnosis and management of incidental exon 43-44 deletion in the dystrophin geneGioia Mastromoro, Daniele Guadagnolo, Enrica Marchionni, et al.
Pageof 16

Showing results (11-20 of 157) with videos related to

Sort By:
Pageof 16
European Journal of Medical Genetics|July 5, 2015
Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndromeM Cristina Digilio, Paolo Versacci, Laura Bernardini, et al.
Journal of Pediatric Hematology/Oncology|July 9, 2003
Medulloblastoma as a secondary malignancy after radiotherapy-free treatment for acute lymphoblastic leukemiaAmalia Schiavetti, Anna Clerico, Maria Debora De Pasquale, et al.
Prenatal Diagnosis|May 29, 2013
Interstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosisAnna Capalbo, Lorenzo Sinibaldi, Laura Bernardini, et al.
Future Oncology (London, England)|May 6, 2024
Dabrafenib-trametinib in BRAF V600-mutated non-small-cell lung cancer: a single center real world experienceAndrea Sbrana, Sabrina Cappelli, Iacopo Petrini, et al.
Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Duplication 18q21.31-q22.2Caterina Ceccarini, Lorenzo Sinibaldi, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
TBX2 gene duplication associated with complex heart defect and skeletal malformationsFrancesca Clementina Radio, Laura Bernardini, Sara Loddo, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
X chromosome monosomy restricted to the left ventricle is not a major cause of isolated hypoplastic left heartLaura Bernardini, Maria Grazia Giuffrida, Paola Francalanci, et al.
European Journal of Medical Genetics|August 14, 2019
A novel mosaic 1q32.1 microduplication identified through Chromosome Microarray Analysis: narrowing the smallest critical region including KDM5B gene found associated with neurodevelopmetal disordersGianmaria Miolo, Maria Grazia Giuffrida, Giuseppe Corona, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 19, 2022
Critical prenatal diagnosis and management of incidental exon 43-44 deletion in the dystrophin geneGioia Mastromoro, Daniele Guadagnolo, Enrica Marchionni, et al.
Pageof 16