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Anna Capalbo

Showing results (11-20 of 30) with videos related to

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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.
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.
American Journal of Medical Genetics. Part A|October 19, 2021
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotypeMarianna Farnè, Laura Bernardini, Anna Capalbo, et al.
Virchows Archiv : an International Journal of Pathology|August 12, 2022
Correction to: Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangementStefano Fratoni, Malgorzata Monika Trawinska, Anna Capalbo, et al.
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.
European Journal of Medical Genetics|January 24, 2007
Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlationLaura Bernardini, Anna Capalbo, Maria Gabriella D'Avanzo, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairsMaria Cristina Digilio, Laura Bernardini, Rita Mingarelli, et al.
Clinical Dysmorphology|December 18, 2008
De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardationMilen Velinov, Antonio Novelli, Hong Gu, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosisViola Alesi, Giuseppe Barrano, Sara Morara, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
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.
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.
American Journal of Medical Genetics. Part A|October 19, 2021
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotypeMarianna Farnè, Laura Bernardini, Anna Capalbo, et al.
Virchows Archiv : an International Journal of Pathology|August 12, 2022
Correction to: Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangementStefano Fratoni, Malgorzata Monika Trawinska, Anna Capalbo, et al.
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.
European Journal of Medical Genetics|January 24, 2007
Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlationLaura Bernardini, Anna Capalbo, Maria Gabriella D'Avanzo, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairsMaria Cristina Digilio, Laura Bernardini, Rita Mingarelli, et al.
Clinical Dysmorphology|December 18, 2008
De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardationMilen Velinov, Antonio Novelli, Hong Gu, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosisViola Alesi, Giuseppe Barrano, Sara Morara, et al.
Pageof 3