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Laura Bernardini

Showing results (31-40 of 157) with videos related to

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Virchows Archiv : an International Journal of Pathology|July 25, 2022
Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangementStefano Fratoni, Malgorzata Monika Trawinska, Anna Capalbo, et al.
Pathology, Research and Practice|December 1, 2019
ALK-negative anaplastic large cell lymphoma with "Hodgkin-like" cytomorphology and nuclear expression of PAX5Stefano Fratoni, Pasquale Niscola, Xiangfeng Frank Zhao, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|December 8, 2022
PARK2 microdeletion in a multiplex family with autism spectrum disorderRita Barone, Lara Cirnigliaro, Lucia Saccuzzo, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Deletion 2p15-16.1 syndrome: case report and reviewPaolo Prontera, Laura Bernardini, Gabriela Stangoni, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 17, 2012
6p25 interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorderMargherita Bozza, Laura Bernardini, Antonio Novelli, et al.
American Journal of Medical Genetics. Part A|July 5, 2013
Homozygous deletion in TUSC3 causing syndromic intellectual disability: a new patientSara Loddo, Valentina Parisi, Viola Doccini, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplicationLaura Bernardini, Marco Castori, Anna Capalbo, et al.
European Journal of Human Genetics : EJHG|March 19, 2009
16p subtelomeric duplication: a clinically recognizable syndromeMaria Cristina Digilio, Laura Bernardini, Anna Capalbo, et al.
Diagnostics (Basel, Switzerland)|January 8, 2023
A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma-Systematic Review of the Literature, Meta-Analysis and Case SeriesGioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, et al.
American Journal of Medical Genetics. Part A|February 28, 2009
2q31.2q32.3 deletion syndrome: report of an adult patientPaolo Prontera, Laura Bernardini, Gabriela Stangoni, et al.
Pageof 16

Showing results (31-40 of 157) with videos related to

Sort By:
Pageof 16
Virchows Archiv : an International Journal of Pathology|July 25, 2022
Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangementStefano Fratoni, Malgorzata Monika Trawinska, Anna Capalbo, et al.
Pathology, Research and Practice|December 1, 2019
ALK-negative anaplastic large cell lymphoma with "Hodgkin-like" cytomorphology and nuclear expression of PAX5Stefano Fratoni, Pasquale Niscola, Xiangfeng Frank Zhao, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|December 8, 2022
PARK2 microdeletion in a multiplex family with autism spectrum disorderRita Barone, Lara Cirnigliaro, Lucia Saccuzzo, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Deletion 2p15-16.1 syndrome: case report and reviewPaolo Prontera, Laura Bernardini, Gabriela Stangoni, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 17, 2012
6p25 interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorderMargherita Bozza, Laura Bernardini, Antonio Novelli, et al.
American Journal of Medical Genetics. Part A|July 5, 2013
Homozygous deletion in TUSC3 causing syndromic intellectual disability: a new patientSara Loddo, Valentina Parisi, Viola Doccini, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplicationLaura Bernardini, Marco Castori, Anna Capalbo, et al.
European Journal of Human Genetics : EJHG|March 19, 2009
16p subtelomeric duplication: a clinically recognizable syndromeMaria Cristina Digilio, Laura Bernardini, Anna Capalbo, et al.
Diagnostics (Basel, Switzerland)|January 8, 2023
A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma-Systematic Review of the Literature, Meta-Analysis and Case SeriesGioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, et al.
American Journal of Medical Genetics. Part A|February 28, 2009
2q31.2q32.3 deletion syndrome: report of an adult patientPaolo Prontera, Laura Bernardini, Gabriela Stangoni, et al.
Pageof 16