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. 2024 Oct 15;18:115. doi: 10.1186/s40246-024-00681-x

Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

Liena Elbaghir Omer Elsayed 1, Norah Ayed AlHarbi 2,, Ashwaq Mohammed Alqarni 3, Huda Hussein Elwasila Eltayeb 1, Noura Mostafa Mohamed Mostafa 1,4, Maha Mohammed Abdulrahim 5, Hadeel Ibrahim Bin Zaid 6, Latifah Mansour Alanzi 7, Sarah Abdullah Ababtain 8, Khawlah Aldulaijan 8, Sheka Yagub Aloyouni 8, Moneeb Abdullah Kassem Othman 9, Mohammad Abdullah Alkheilewi 10, Adel Mohammed Binduraihem 8, Hadeel Abdollah Alrukban 11, Hiba Yousif Ahmed 12, Faten Abdullah AlRadini 13, Hadil Mohammad Alahdal 14, Aziza Mufareh Mushiba 12,15, Omaima Abdulazeem Alzaher 16
PMCID: PMC11475645  PMID: 39407347

Human Genomics (2024) 18:95

10.1186/s40246-024-00662-0

The original article presents two errors which the authors wish to clarify:

  1. The captions for Figs. 1 and 2 are mistakenly swapped by the production team handling this article and should instead be the other way around.

  2. In numerous affiliations where relevant, the word ‘bint’ should instead be presented with a lower-case ‘b’ instead of upper-case.

Footnotes

The online version of the original article can be found at 10.1186/s40246-024-00662-0.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.


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