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Clinical and molecular features of four families with CLDN10-related HELIX syndrome.
Eur J Med Genet. 2023 Dec;66(12):104886. doi: 10.1016/j.ejmg.2023.104886. Epub 2023 Nov 18.
Eur J Med Genet. 2023.
PMID: 37984702
Review.
Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome.
Altassan R, Qudair A, Alokaili R, Alhasan K, Faqeih EA, Alhashem A, Alowain M, Alsayed M, Rahbeeni Z, Albadi L, Alkuraya FS, Anderson EN, Rajan D, Pandey UB.
Altassan R, et al. Among authors: qudair a.
Am J Med Genet A. 2022 Oct;188(10):2932-2940. doi: 10.1002/ajmg.a.62894. Epub 2022 Jul 21.
Am J Med Genet A. 2022.
PMID: 35861185
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Challenges of implementing a standardized process for discharge summaries (5 years experience).
Almidani E, Qudair A, Khadawardi E, Alshareef T, Shoura S, Alobari R, Alhajjar S, Almofada S.
Almidani E, et al. Among authors: qudair a.
Int J Pediatr Adolesc Med. 2017 Sep;4(3):115-118. doi: 10.1016/j.ijpam.2017.06.001. Epub 2017 Nov 27.
Int J Pediatr Adolesc Med. 2017.
PMID: 30805513
Free PMC article.
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Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract.
Patel N, Anand D, Monies D, Maddirevula S, Khan AO, Algoufi T, Alowain M, Faqeih E, Alshammari M, Qudair A, Alsharif H, Aljubran F, Alsaif HS, Ibrahim N, Abdulwahab FM, Hashem M, Alsedairy H, Aldahmesh MA, Lachke SA, Alkuraya FS.
Patel N, et al. Among authors: qudair a.
Hum Genet. 2017 Feb;136(2):205-225. doi: 10.1007/s00439-016-1747-6. Epub 2016 Nov 22.
Hum Genet. 2017.
PMID: 27878435
Free PMC article.
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