Cargando…
Application of molecular genetics techniques for detecting deleted segmental aneuploidy in Williams Syndrome
Autores principales: | Magbooli, Afaf, Huwait, Etimad, Hussein, Ibtessam R, AlQahtani, Mohammed |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075607/ http://dx.doi.org/10.1186/1471-2164-15-S2-P34 |
Ejemplares similares
-
Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia
por: Hussein, I. R., et al.
Publicado: (2016) -
Frequent microdeletions in conventional papillary thyroid carcinoma detected by high-density oligonucleotide microarrays
por: Al-Ahmadi, Alaa, et al.
Publicado: (2014) -
Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi Arabia
por: Hussein, Ibtessam Ramzi, et al.
Publicado: (2014) -
The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniques
por: Bahamat, Abeer A, et al.
Publicado: (2014) -
High-density microarray expression profiling in conventional papillary thyroid carcinomas with versus without a BRAF mutation
por: Alotibi, Reem, et al.
Publicado: (2014)