Cargando…
Investigation into the Importance of genes encoding ciliary proteins in congenital heart disease using whole exome sequencing
Autores principales: | Hartill, V, Logan, C, Parry, DA, Szymanska, K, Ashcroft, K, English, K, Prescott, K, Dobbie, A, Barwick, S, Bennett, C, Goodship, J, Sheridan, E, Johnson, C |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518900/ http://dx.doi.org/10.1186/2046-2530-4-S1-P9 |
Ejemplares similares
-
Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia
por: Gileles-Hillel, Alex, et al.
Publicado: (2020) -
Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia
por: Marshall, Christian R., et al.
Publicado: (2015) -
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
por: Leung, Gordon K C, et al.
Publicado: (2018) -
Biochemical characterization of transmembrane proteins (TMEMs) in the ciliary transition zone
por: Shoaib, E, et al.
Publicado: (2015) -
An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families
por: Guo, Ting, et al.
Publicado: (2017)