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Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles.
J Clin Invest. 2024 Nov 15;134(22):e170669. doi: 10.1172/JCI170669.
J Clin Invest. 2024.
PMID: 39545410
Free PMC article.
Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population.
Vallian Broojeni J, Kazemi A, Rezaei H, Vallian S.
Vallian Broojeni J, et al.
PLoS One. 2023 Aug 10;18(8):e0289247. doi: 10.1371/journal.pone.0289247. eCollection 2023.
PLoS One. 2023.
PMID: 37561809
Free PMC article.
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