Author/Creator: Albarry, Maan Abdullah - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Albarry, Maan Abdullah

1. Novel homozygous loss-of-function mutations in RP1 and RP1L1 genes in retinitis pigmentosa patients. (2nd November 2019)

Authors:: Albarry, Maan Abdullah; Hashmi, Jamil Amjad; Alreheli, Ahdab Qasem; Albalawi, Alia M.; Khan, Bushra; Ramzan, Khushnooda; Basit, Sulman
Journal:: Ophthalmic genetics
Issue:: Volume 40:Number 6(2019)
Page Start:: 507
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. (28th May 2017)

Authors:: Hashmi, Jamil Amjad; Albarry, Maan Abdullah; Almatrafi, Ahmed M.; Albalawi, Alia M.; Mahmood, Amer; Basit, Sulman
Journal:: Congenital anomalies
Issue:: Volume 58:Number 1(2018)
Page Start:: 10
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗