Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype
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Published in | Human genomics Vol. 18; no. 1; pp. 115 - 2 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
15.10.2024
BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1479-7364 1473-9542 1479-7364 |
DOI | 10.1186/s40246-024-00681-x |
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ArticleNumber | 115 |
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Author | Othman, Moneeb Abdullah Kassem Alkheilewi, Mohammad Abdullah Abdulrahim, Maha Mohammed Alahdal, Hadil Mohammad Alzaher, Omaima Abdulazeem Ababtain, Sarah Abdullah Aloyouni, Sheka Yagub Mostafa, Noura Mostafa Mohamed Alanzi, Latifah Mansour Eltayeb, Huda Hussein Elwasila Binduraihem, Adel Mohammed AlRadini, Faten Abdullah AlHarbi, Norah Ayed Alqarni, Ashwaq Mohammed Alrukban, Hadeel Abdollah Mushiba, Aziza Mufareh Elsayed, Liena Elbaghir Omer Zaid, Hadeel Ibrahim Bin Ahmed, Hiba Yousif Aldulaijan, Khawlah |
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References | 39232803 - Hum Genomics. 2024 Sep 4;18(1):95. doi: 10.1186/s40246-024-00662-0 |
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Title | Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype |
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