Cargando…
Genetics of inherited cardiocutaneous syndromes: a review
The life of a human being originates as a single cell which, under the influence of certain factors, divides sequentially into multiple cells that subsequently become committed to develop and differentiate into the different structures and organs. Alterations occurring early on in the development pr...
Autores principales: | Bardawil, Tara, Khalil, Samar, Bergqvist, Christina, Abbas, Ossama, Kibbi, Abdul Ghani, Bitar, Fadi, Nemer, Georges, Kurban, Mazen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133403/ https://www.ncbi.nlm.nih.gov/pubmed/27933191 http://dx.doi.org/10.1136/openhrt-2016-000442 |
Ejemplares similares
-
Scabies in the age of increasing drug resistance
por: Khalil, Samar, et al.
Publicado: (2017) -
Identification of Several Mutations in ATP2C1 in Lebanese Families: Insight into the Pathogenesis of Hailey-Hailey Disease
por: Btadini, Waed, et al.
Publicado: (2015) -
A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases
por: Khalil, Athar, et al.
Publicado: (2017) -
A novel mutation in the HPGD gene results in the unusual phenotype of palmoplantar keratoderma with digital clubbing and hyperhidrosis
por: Stephan, Carla, et al.
Publicado: (2018) -
A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
por: Khalil, Athar, et al.
Publicado: (2017)