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Forensic Science International
|
June 13, 2016
Human identification by lice: A Next Generation Sequencing challenge
Elena Pilli, Alessandro Agostino, Debora Vergani, et al.
Hemasphere
|
July 17, 2024
Prospective genetic germline evaluation in a consecutive group of adult patients aged <60 years with myelodysplastic syndromes
Enrico Attardi, Lucia Tiberi, Giorgio Mattiuz, et al.
The Journal of Pathology
|
June 14, 2017
SMARCA4 inactivating mutations cause concomitant Coffin-Siris syndrome, microphthalmia and small-cell carcinoma of the ovary hypercalcaemic type
Edoardo Errichiello, Noor Mustafa, Annalisa Vetro, et al.
International Journal of Molecular Sciences
|
May 28, 2022
Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome
Viviana Palazzo, Valentina Raglianti, Samuela Landini, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2017
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome
Annalisa Vetro, Salvatore Savasta, Annalisa Russo Raucci, et al.
Pathologica
|
December 27, 2025
The contribution of methylation profiling in neuropathological diagnosis of central nervous system tumors in children, adolescent and young adults
Anna Maria Buccoliero, Laura Giunti, Mirko Scagnet, et al.
American Journal of Medical Genetics. Part A
|
November 6, 2025
Genotypes and Phenotypes of Patients With TSPEAR-Related Disorder: Evidence of a Predominant Dental Phenotype
Debora Vergani, Lucia Tiberi, Annarita Giliberti, et al.
Scientific Reports
|
July 4, 2024
Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights
Giacomo M Bacci, Elisa Marziali, Sara Bargiacchi, et al.
Human Genetics
|
December 18, 2020
Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes
Aldesia Provenzano, Andrea La Barbera, Mirko Scagnet, et al.
Journal of the American Society of Nephrology : JASN
|
February 8, 2023
A Clinical Workflow for Cost-Saving High-Rate Diagnosis of Genetic Kidney Diseases
Francesca Becherucci, Samuela Landini, Viviana Palazzo, et al.
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Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Forensic Science International
|
June 13, 2016
Human identification by lice: A Next Generation Sequencing challenge
Elena Pilli, Alessandro Agostino, Debora Vergani, et al.
Hemasphere
|
July 17, 2024
Prospective genetic germline evaluation in a consecutive group of adult patients aged <60 years with myelodysplastic syndromes
Enrico Attardi, Lucia Tiberi, Giorgio Mattiuz, et al.
The Journal of Pathology
|
June 14, 2017
SMARCA4 inactivating mutations cause concomitant Coffin-Siris syndrome, microphthalmia and small-cell carcinoma of the ovary hypercalcaemic type
Edoardo Errichiello, Noor Mustafa, Annalisa Vetro, et al.
International Journal of Molecular Sciences
|
May 28, 2022
Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome
Viviana Palazzo, Valentina Raglianti, Samuela Landini, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2017
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome
Annalisa Vetro, Salvatore Savasta, Annalisa Russo Raucci, et al.
Pathologica
|
December 27, 2025
The contribution of methylation profiling in neuropathological diagnosis of central nervous system tumors in children, adolescent and young adults
Anna Maria Buccoliero, Laura Giunti, Mirko Scagnet, et al.
American Journal of Medical Genetics. Part A
|
November 6, 2025
Genotypes and Phenotypes of Patients With TSPEAR-Related Disorder: Evidence of a Predominant Dental Phenotype
Debora Vergani, Lucia Tiberi, Annarita Giliberti, et al.
Scientific Reports
|
July 4, 2024
Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights
Giacomo M Bacci, Elisa Marziali, Sara Bargiacchi, et al.
Human Genetics
|
December 18, 2020
Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes
Aldesia Provenzano, Andrea La Barbera, Mirko Scagnet, et al.
Journal of the American Society of Nephrology : JASN
|
February 8, 2023
A Clinical Workflow for Cost-Saving High-Rate Diagnosis of Genetic Kidney Diseases
Francesca Becherucci, Samuela Landini, Viviana Palazzo, et al.
Page
of 2