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Page 1
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management.
Genes (Basel). 2022 Nov 23;13(12):2192. doi: 10.3390/genes13122192.
Genes (Basel). 2022.
PMID: 36553459
Free PMC article.
Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies.
Azab B, Dardas Z, Aburizeg D, Al-Bdour M, Abu-Ameerh M, Saleh T, Barham R, Maswadi R, Ababneh NA, Alsalem M, Zouk H, Amr S, Awidi A.
Azab B, et al. Among authors: aburizeg d.
Genes (Basel). 2021 Apr 19;12(4):593. doi: 10.3390/genes12040593.
Genes (Basel). 2021.
PMID: 33921607
Free PMC article.
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Investigating the genetic profile of familial atypical cystic fibrosis patients (DeltaF508-CFTR) with neonatal biliary atresia.
Altamimi E, Rabab'h O, Aburizeg D, Akasheh L, Dardas Z, Srour L, Awad H, Azab B.
Altamimi E, et al. Among authors: aburizeg d.
J Appl Genet. 2023 Feb;64(1):71-80. doi: 10.1007/s13353-022-00729-5. Epub 2022 Oct 7.
J Appl Genet. 2023.
PMID: 36205856
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Potential Composite Digenic Contribution of NPC1 and NOD2 Leading to Atypical Lethal Niemann-Pick Type C with Initial Crohn's Disease-like Presentation: Genotype-Phenotype Correlation Study.
Azab B, Rabab'h O, Aburizeg D, Mohammad H, Dardas Z, Mustafa L, Khasawneh RA, Awad H, Hatmal MM, Altamimi E.
Azab B, et al. Among authors: aburizeg d.
Genes (Basel). 2022 May 29;13(6):973. doi: 10.3390/genes13060973.
Genes (Basel). 2022.
PMID: 35741735
Free PMC article.
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TBX5 variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defects.
Azab B, Aburizeg D, Ji W, Jeffries L, Isbeih NJ, Al-Akily AS, Mohammad H, Osba YA, Shahin MA, Dardas Z, Hatmal MM, Al-Ammouri I, Lakhani S.
Azab B, et al. Among authors: aburizeg d.
Mol Med Rep. 2022 Jun;25(6):210. doi: 10.3892/mmr.2022.12726. Epub 2022 May 6.
Mol Med Rep. 2022.
PMID: 35514310
Free PMC article.
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