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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Am J Hum Genet. 2024 Jan 4;111(1):200-210. doi: 10.1016/j.ajhg.2023.11.012. Epub 2023 Dec 20.
Am J Hum Genet. 2024.
PMID: 38118446
Free PMC article.
Gene dosage analysis of proximal spinal muscular atrophy carriers using real-time PCR.
Abbaszadegan MR, Keify F, Ashrafzadeh F, Farshchian M, Khadivi-Zand F, Teymoorzadeh MN, Mojahedi F, Ebrahimzadeh R, Ahadian M.
Abbaszadegan MR, et al. Among authors: khadivi zand f.
Arch Iran Med. 2011 May;14(3):188-91.
Arch Iran Med. 2011.
PMID: 21529108
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Rare gross deletion in T-cell immune regulator-1 gene in Iranian family with infantile malignant osteopetrosis.
Abbaszadegan MR, Modarresi A, Khadivi-Zand F, Velayati A.
Abbaszadegan MR, et al. Among authors: khadivi zand f.
Saudi Med J. 2008 Oct;29(10):1494-6.
Saudi Med J. 2008.
PMID: 18946580
Review.
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