Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ghassan Zidan"'
Autor:
Ali Hellani, Nancy L. Sicotte, Ghassan Zidan, Thomas M. Bosley, Ibrahim A. Alorainy, Khaled K. Abu-Amero, Kyle C. Kern, Mustafa A. Salih
Publikováno v:
Ophthalmic Genetics. 31:147-154
Neuro-ophthalmologic and neuroimaging features of partial chromosome 18p deletion syndromes have not yet been fully described.Careful neuro-ophthalmologic and neuroimaging evaluation of a young woman with a partial 18p deletion, including 3 Tesla MRI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4403974fe597ca278e6acbdd37231ab1
https://doi.org/10.3109/13816810.2010.492817
https://doi.org/10.3109/13816810.2010.492817
Autor:
Thomas M. Bosley, Ibrahim A. Alorainy, Abdulkarim Al Hussain, Majed al Obailan, Ali Hellani, Khaled K. Abu-Amero, Mustafa A. Salih, Ghassan Zidan
Publikováno v:
Ophthalmic genetics. 31(1)
To correlate the clinical phenotype with the genotype of a boy with a terminal deletion of chromosome 6q and to compare these observations to previous reports of 6q deletions and review of the literature.Careful clinical evaluation, conventional cyto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5464a82bd5057ab8706c119583ac85e
https://pubmed.ncbi.nlm.nih.gov/20141352
https://pubmed.ncbi.nlm.nih.gov/20141352
Autor:
Ali Hellani, Mohammad Z. Seidahmed, Khaled K. Abu-Amero, Thomas M. Bosley, Mustafa A. Salih, Tageldin S Elmalik, Ghassan Zidan
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 11, Iss 1, p 135 (2010)
BMC Medical Genetics, Vol 11, Iss 1, p 135 (2010)
Background Previous studies focusing on candidate genes and chromosomal regions identified several copy number variations (CNVs) associated with increased risk of autism or autism spectrum disorders (ASD). Case Presentation We describe a 17-year-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa97b14e3193e7cd51d8f0c161c0028