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

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype ; volume:18 ; number:1 ; day:4 ; month:9 ; year:2024 ; pages:1-10 ; date:12.2024
Human genomics ; 18, Heft 1 (4.9.2024), 1-10, 12.2024

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

Contributor: SpringerLink (Online service)

DOI: 10.1186/s40246-024-00662-0

URN: urn:nbn:de:101:1-2501022155024.560966443323

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:34 AM CEST

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Associated

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

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

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Other Objects (12)

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

Revisiting dandy–Walker malformation with associated neurofibromatosis

Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report

RARE ASSOCIATION OF DOWN SYNDROME WITH DANDY WALKER MALFORMATION

Dandy-Walker malformation in methylmalonic acidemia: a rare case report

Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review

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

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Revisiting dandy–Walker malformation with associated neurofibromatosis

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