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

Liena Elbaghir Omer Elsayed, Norah Ayed AlHarbi, Ashwaq Mohammed Alqarni, Huda Hussein Elwasila Eltayeb, Noura Mostafa Mohamed Mostafa, Maha Mohammed Abdulrahim, Hadeel Ibrahim Bin Zaid, Latifah Mansour Alanzi, Sarah Abdullah Ababtain, Khawlah Aldulaijan, Sheka Yagub Aloyouni, Moneeb Abdullah Kassem Othman, Mohammad Abdullah Alkheilewi, Adel Mohammed Binduraihem, Hadeel Abdollah Alrukban, Hiba Yousif Ahmed, Faten Abdullah AlRadini, Hadil Mohammad Alahdal, Aziza Mufareh Mushiba, Omaima Abdulazeem Alzaher

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DOI: 10.1186/s40246-024-00662-0
Published: 2024-09-04
Container: Human Genomics
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1186/s40246-024-00662-0,
  title = {Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype},
  author = {Liena Elbaghir Omer Elsayed and Norah Ayed AlHarbi and Ashwaq Mohammed Alqarni and Huda Hussein Elwasila Eltayeb and Noura Mostafa Mohamed Mostafa and Maha Mohammed Abdulrahim and Hadeel Ibrahim Bin Zaid and Latifah Mansour Alanzi and Sarah Abdullah Ababtain and Khawlah Aldulaijan and Sheka Yagub Aloyouni and Moneeb Abdullah Kassem Othman and Mohammad Abdullah Alkheilewi and Adel Mohammed Binduraihem and Hadeel Abdollah Alrukban and Hiba Yousif Ahmed and Faten Abdullah AlRadini and Hadil Mohammad Alahdal and Aziza Mufareh Mushiba and Omaima Abdulazeem Alzaher},
  year = {2024},
  journal = {Human Genomics},
  doi = {10.1186/s40246-024-00662-0},
  url = {https://doi.org/10.1186/s40246-024-00662-0}
}

RIS

TY  - JOUR
TI  - Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype
AU  - Liena Elbaghir Omer Elsayed
AU  - Norah Ayed AlHarbi
AU  - Ashwaq Mohammed Alqarni
AU  - Huda Hussein Elwasila Eltayeb
AU  - Noura Mostafa Mohamed Mostafa
AU  - Maha Mohammed Abdulrahim
AU  - Hadeel Ibrahim Bin Zaid
AU  - Latifah Mansour Alanzi
AU  - Sarah Abdullah Ababtain
AU  - Khawlah Aldulaijan
AU  - Sheka Yagub Aloyouni
AU  - Moneeb Abdullah Kassem Othman
AU  - Mohammad Abdullah Alkheilewi
AU  - Adel Mohammed Binduraihem
AU  - Hadeel Abdollah Alrukban
AU  - Hiba Yousif Ahmed
AU  - Faten Abdullah AlRadini
AU  - Hadil Mohammad Alahdal
AU  - Aziza Mufareh Mushiba
AU  - Omaima Abdulazeem Alzaher
PY  - 2024
JO  - Human Genomics
DO  - 10.1186/s40246-024-00662-0
UR  - https://doi.org/10.1186/s40246-024-00662-0
ER  -

APA

Elsayed, L. E. O., AlHarbi, N. A., Alqarni, A. M., Eltayeb, H. H. E., Mostafa, N. M. M., Abdulrahim, M. M., Zaid, H. I. B., Alanzi, L. M., Ababtain, S. A., Aldulaijan, K., Aloyouni, S. Y., Othman, M. A. K., Alkheilewi, M. A., Binduraihem, A. M., Alrukban, H. A., Ahmed, H. Y., AlRadini, F. A., Alahdal, H. M., Mushiba, A. M., & Alzaher, O. A. (2024). Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype. Human Genomics. https://doi.org/10.1186/s40246-024-00662-0

Source records

crossref · retrieved 2026-09-26T18:02:21.786Z