Cargando…
Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population
BACKGROUND: Retinoblastoma is the most common intraocular tumor in childhood and mutation in the RB1 gene will trigger the tumorigenesis. So far, a wide range of the mutations along the length of RB1 gene have been reported. However, some could not be detected by common detection methods. In such co...
Autores principales: | Zahery, Saman Mohamad, Saliminejad, Kioomars, Khorshid, Hamid Reza Khorram, Ahani, Ali |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Avicenna Research Institute
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558219/ https://www.ncbi.nlm.nih.gov/pubmed/23407622 |
Ejemplares similares
-
Discrepancy in the results of Y chromosome microdeletions in an Iranian population
por: Saliminejad, Kioomars, et al.
Publicado: (2011) -
Methodological errors in screening of Yq microdeletion in Iranian azoospermic men
por: Saliminejad, Kioomars, et al.
Publicado: (2012) -
Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification
por: Ahani, Ali, et al.
Publicado: (2013) -
Association study of Glutathione S-Transferase polymorphisms and risk of endometriosis in an Iranian population
por: Hassani, Mina, et al.
Publicado: (2016) -
Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification
por: Ashtari, Fereshteh, et al.
Publicado: (2013)