Cargando…
The added value of WES reanalysis in the field of genetic diagnosis: lessons learned from 200 exomes in the Lebanese population
BACKGROUND: The past few decades have witnessed a tremendous development in the field of genetics. The implementation of next generation sequencing (NGS) technologies revolutionized the field of molecular biology and made the genetic information accessible at a large scale. However, connecting a rar...
Autores principales: | Jalkh, Nadine, Corbani, Sandra, Haidar, Zahraa, Hamdan, Nadine, Farah, Elias, Abou Ghoch, Joelle, Ghosn, Rouba, Salem, Nabiha, Fawaz, Ali, Djambas Khayat, Claudia, Rajab, Mariam, Mourani, Chebl, Moukarzel, Adib, Rassi, Simon, Gerbaka, Bernard, Mansour, Hicham, Baassiri, Malek, Dagher, Rawane, Breich, David, Mégarbané, André, Desvignes, Jean Pierre, Delague, Valérie, Mehawej, Cybel, Chouery, Eliane |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341681/ https://www.ncbi.nlm.nih.gov/pubmed/30665423 http://dx.doi.org/10.1186/s12920-019-0474-y |
Ejemplares similares
-
First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene
por: Chebly, Alain, et al.
Publicado: (2018) -
Actionable Exomic Secondary Findings in 280 Lebanese Participants
por: Jalkh, Nadine, et al.
Publicado: (2020) -
Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients
por: Choucair, Nancy, et al.
Publicado: (2015) -
The Impairment of MAGMAS Function in Human Is Responsible for a Severe Skeletal Dysplasia
por: Mehawej, Cybel, et al.
Publicado: (2014) -
PCDH19 in Males: Are Hemizygous Variants Linked to Autism?
por: Chouery, Eliane, et al.
Publicado: (2023)