ArticleNumber 115
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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  givenname: Norah Ayed
  surname: AlHarbi
  fullname: AlHarbi, Norah Ayed
  email: Noaalharbi@pnu.edu.sa
  organization: Department of Internal Medicine, College of Medicine, Princess Nourah bint Abdulrahman University
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  givenname: Ashwaq Mohammed
  surname: Alqarni
  fullname: Alqarni, Ashwaq Mohammed
  organization: Foundation Year of Health Colleges, Princess Nourah bint Abdulrahman University
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  givenname: Huda Hussein Elwasila
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  fullname: Eltayeb, Huda Hussein Elwasila
  organization: Department of Basic Sciences, College of Medicine, Princess Nourah bint Abdulrahman University
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  surname: Mostafa
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  organization: Department of Basic Sciences, College of Medicine, Princess Nourah bint Abdulrahman University, Medical Biochemistry Department, Faculty of Medicine, Zagazig University
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  givenname: Maha Mohammed
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  fullname: Abdulrahim, Maha Mohammed
  organization: Research and Academic Accreditation, Academic Affairs, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University
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  givenname: Hadeel Ibrahim Bin
  surname: Zaid
  fullname: Zaid, Hadeel Ibrahim Bin
  organization: Out-Patient department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University
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  surname: Alanzi
  fullname: Alanzi, Latifah Mansour
  organization: Department of Pathology and Laboratory Medicine, King Abdullah Bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University
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  givenname: Sarah Abdullah
  surname: Ababtain
  fullname: Ababtain, Sarah Abdullah
  organization: Genetics Section, Research Department, Health Sciences Research Center, Princess Nourah bint Abdulrahman University
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  fullname: Aldulaijan, Khawlah
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  fullname: Aloyouni, Sheka Yagub
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  organization: Health Support Services Centre, Ministry of Health
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  givenname: Adel Mohammed
  surname: Binduraihem
  fullname: Binduraihem, Adel Mohammed
  organization: Genetics Section, Research Department, Health Sciences Research Center, Princess Nourah bint Abdulrahman University
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  fullname: Alrukban, Hadeel Abdollah
  organization: Pediatric Department, Division of Genetic and Metabolic, Prince Sultan Military Medical City
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  organization: Pediatrics department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University
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  givenname: Faten Abdullah
  surname: AlRadini
  fullname: AlRadini, Faten Abdullah
  organization: Family and Community Medicine Department, College of Medicine, Princess Nourah bint Abdulrahman University
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  givenname: Hadil Mohammad
  surname: Alahdal
  fullname: Alahdal, Hadil Mohammad
  organization: Department of Biology, College of Science, Princes Nourah bint Abdulrahman University
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  givenname: Aziza Mufareh
  surname: Mushiba
  fullname: Mushiba, Aziza Mufareh
  organization: Pediatrics department, King Abdullah bin Abdulaziz University Hospital, Princess Nourah bint Abdulrahman University, Section of Medical Genetics, Children’s Hospital, King Fahad Medical City
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  givenname: Omaima Abdulazeem
  surname: Alzaher
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  organization: Pediatric Department, College of Medicine, Princess Nourah bint Abdulrahman University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39407347$$D View this record in MEDLINE/PubMed
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PublicationTitle Human genomics
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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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SubjectTerms Bioinformatics
Biomedical and Life Sciences
Biomedicine
Correction
Human Genetics
Proteomics
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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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