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Page 1
Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients.
Hum Mutat. 2022 Dec;43(12):e24-e37. doi: 10.1002/humu.24480. Epub 2022 Oct 8.
Hum Mutat. 2022.
PMID: 36177613
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
Al-Mousa H, Abouelhoda M, Monies DM, Al-Tassan N, Al-Ghonaium A, Al-Saud B, Al-Dhekri H, Arnaout R, Al-Muhsen S, Ades N, Elshorbagi S, Al Gazlan S, Sheikh F, Dasouki M, El-Baik L, Elamin T, Jaber A, Kheir O, El-Kalioby M, Subhani S, Al Idrissi E, Al-Zahrani M, Alhelale M, Alnader N, Al-Otaibi A, Kattan R, Al Abdelrahman K, Al Breacan MM, Bin Humaid FS, Wakil SM, Alzayer F, Al-Dusery H, Faquih T, Al-Hissi S, Meyer BF, Hawwari A.
Al-Mousa H, et al.
J Allergy Clin Immunol. 2016 Jun;137(6):1780-1787. doi: 10.1016/j.jaci.2015.12.1310. Epub 2016 Feb 23.
J Allergy Clin Immunol. 2016.
PMID: 26915675
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Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
Al-Hamed MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F.
Al-Hamed MH, et al. Among authors: alotaibi a.
Hum Genet. 2022 Jan;141(1):101-126. doi: 10.1007/s00439-021-02406-9. Epub 2021 Dec 1.
Hum Genet. 2022.
PMID: 34853893
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Perceptions of Arabian Gulf Residents and Citizens about Physical Activity and Social Media Awareness Campaigns: A Qualitative Study.
Alkhaldi G, Alotaibi A, Alkasabi R, Alsadhan N, Alageel S.
Alkhaldi G, et al. Among authors: alotaibi a.
Behav Sci (Basel). 2024 Feb 23;14(3):174. doi: 10.3390/bs14030174.
Behav Sci (Basel). 2024.
PMID: 38540477
Free PMC article.
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