Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

Abstract Background This study aimed to delineate the clinical phenotype of patients with 9p deletions, pinpoint the chromosomal breakpoints, and identify the critical region for trigonocephaly, which is a frequent finding in 9p terminal deletion. Methods We investigated a cohort of nine patients wi...

Full description

Saved in:
Bibliographic Details
Main Authors: Amal M. Mohamed, Alaa K. Kamel, Maha M. Eid, Ola M. Eid, Mona Mekkawy, Shymaa H. Hussein, Maha S. Zaki, Samira Esmail, Hanan H. Afifi, Ghada Y. El‐Kamah, Ghada A. Otaify, Heba Ahmed El‐Awady, Aya Elaidy, Mahmoud Y. Essa, Mona El‐Ruby, Engy A. Ashaat, Saida A. Hammad, Inas Mazen, Ghada M. H. Abdel‐Salam, Mona Aglan, Samia Temtamy
Format: article
Language:EN
Published: Wiley 2021
Subjects:
9p deletion
ambiguous genitalia
autism
brain anomalies
trigonocephaly
Genetics
QH426-470
Online Access:https://doaj.org/article/2bfe665e28c74ca3b3ab3b493e122b7b
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://doaj.org/article/2bfe665e28c74ca3b3ab3b493e122b7b

Similar Items