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Biallelic ZNFX1 variants are associated with a spectrum of immuno-hematological abnormalities.
Clin Genet. 2022 Feb;101(2):247-254. doi: 10.1111/cge.14081. Epub 2021 Nov 6.
Clin Genet. 2022.
PMID: 34708404
Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects.
Ng CK, Shboul M, Taverniti V, Bonnard C, Lee H, Eskin A, Nelson SF, Al-Raqad M, Altawalbeh S, Séraphin B, Reversade B.
Ng CK, et al.
Hum Mol Genet. 2015 Jun 1;24(11):3163-71. doi: 10.1093/hmg/ddv067. Epub 2015 Feb 24.
Hum Mol Genet. 2015.
PMID: 25712129
Free PMC article.
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A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
Chia PH, Zhong FL, Niwa S, Bonnard C, Utami KH, Zeng R, Lee H, Eskin A, Nelson SF, Xie WH, Al-Tawalbeh S, El-Khateeb M, Shboul M, Pouladi MA, Al-Raqad M, Reversade B.
Chia PH, et al. Among authors: al tawalbeh s.
Elife. 2018 May 22;7:e32451. doi: 10.7554/eLife.32451.
Elife. 2018.
PMID: 29784083
Free PMC article.
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Congenital Partial Arhinia.
Altawalbeh A, AlHaji M, Qatawneh M, AlSharadqeh A, AlBataineh M, Almestarihi L, AlTawalbeh S, AlMbaidin L.
Altawalbeh A, et al.
Mater Sociomed. 2022 Sep;34(3):225-227. doi: 10.5455/msm.2022.34.225-227.
Mater Sociomed. 2022.
PMID: 36310750
Free PMC article.
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Glycemic Control and Its Relationship with Diabetes Self-Care Behaviors Among Patients with Type 2 Diabetes in Northern Jordan: A Cross-Sectional Study.
Almomani MH, Al-Tawalbeh S.
Almomani MH, et al. Among authors: al tawalbeh s.
Patient Prefer Adherence. 2022 Feb 19;16:449-465. doi: 10.2147/PPA.S343214. eCollection 2022.
Patient Prefer Adherence. 2022.
PMID: 35221675
Free PMC article.
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