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Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.
Hum Genomics. 2024 Oct 15;18(1):115. doi: 10.1186/s40246-024-00681-x.
Hum Genomics. 2024.
PMID: 39407347
Free PMC article.
No abstract available.
Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.
Elsayed LEO, AlHarbi NA, Alqarni AM, Eltayeb HHE, Mostafa NMM, Abdulrahim MM, Zaid HIB, Alanzi LM, Ababtain SA, Aldulaijan K, Aloyouni SY, Othman MAK, Alkheilewi MA, Binduraihem AM, Alrukban HA, Ahmed HY, AlRadini FA, Alahdal HM, Mushiba AM, Alzaher OA.
Elsayed LEO, et al. Among authors: ababtain sa.
Hum Genomics. 2024 Sep 4;18(1):95. doi: 10.1186/s40246-024-00662-0.
Hum Genomics. 2024.
PMID: 39232803
Free PMC article.
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Molecular Background of RhD-positive and RhD-negative Phenotypes in a Saudi Population.
Alalshaikh MA, Alsughayir AH, Alsaif AS, Ababtain SA, Aloyouni SY, Aldilaijan KE, Alsubaie SF.
Alalshaikh MA, et al. Among authors: ababtain sa.
Saudi J Med Med Sci. 2024 Jul-Sep;12(3):210-215. doi: 10.4103/sjmms.sjmms_664_23. Epub 2024 Jun 20.
Saudi J Med Med Sci. 2024.
PMID: 39055072
Free PMC article.
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