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Nephrotic syndrome: Pretibial epidermolysis bullosa in a patient with CD151 tetraspanin defect: A case report.
Int J Health Sci (Qassim). 2024 Jan-Feb;18(1):35-40.
Int J Health Sci (Qassim). 2024.
PMID: 38188895
Free PMC article.
Reclassifying variations of unknown significance in diseases affecting Saudi Arabia's population reveal new associations.
Al Eissa MM, Alotibi RS, Alhaddad B, Aloraini T, Samman MS, AlAsiri A, Abouelhoda M, AlQahtani AS.
Al Eissa MM, et al. Among authors: alotibi rs.
Front Genet. 2023 Nov 1;14:1250317. doi: 10.3389/fgene.2023.1250317. eCollection 2023.
Front Genet. 2023.
PMID: 38028588
Free PMC article.
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Prospect of genetic disorders in Saudi Arabia.
Alqahtani AS, Alotibi RS, Aloraini T, Almsned F, Alassali Y, Alfares A, Alhaddad B, Al Eissa MM.
Alqahtani AS, et al. Among authors: alotibi rs.
Front Genet. 2023 Sep 20;14:1243518. doi: 10.3389/fgene.2023.1243518. eCollection 2023.
Front Genet. 2023.
PMID: 37799141
Free PMC article.
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The diagnostic yield of CGH and WES in neurodevelopmental disorders.
Alotibi RS, Sannan NS, AlEissa M, Aldriwesh MG, Al Tuwaijri A, Akiel MA, Almutairi M, Alsamer A, Altharawi N, Aljawfan G, Alotiabi B, AlBlawi MA, Alfares A.
Alotibi RS, et al.
Front Pediatr. 2023 Mar 1;11:1133789. doi: 10.3389/fped.2023.1133789. eCollection 2023.
Front Pediatr. 2023.
PMID: 36937954
Free PMC article.
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