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

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 with chro...

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Detalles Bibliográficos
Autores principales: Mohamed, Amal M., Kamel, Alaa K., Eid, Maha M., Eid, Ola M., Mekkawy, Mona, Hussein, Shymaa H., Zaki, Maha S., Esmail, Samira, Afifi, Hanan H., El‐Kamah, Ghada Y., Otaify, Ghada A., El‐Awady, Heba Ahmed, Elaidy, Aya, Essa, Mahmoud Y., El‐Ruby, Mona, Ashaat, Engy A., Hammad, Saida A., Mazen, Inas, Abdel‐Salam, Ghada M. H., Aglan, Mona, Temtamy, Samia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606205/
https://www.ncbi.nlm.nih.gov/pubmed/34609792
http://dx.doi.org/10.1002/mgg3.1829

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606205/
https://www.ncbi.nlm.nih.gov/pubmed/34609792
http://dx.doi.org/10.1002/mgg3.1829

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