Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mahmoud Y. Essa"'
Autor:
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
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
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. Me
Externí odkaz:
https://doaj.org/article/2bfe665e28c74ca3b3ab3b493e122b7b
Autor:
Maha M. Eid, Mahmoud Y Essa, Aya Elaidy, Alaa K. Kamel, Mona O. El-Ruby, Samia A. Temtamy, Saida A Hammad, Ghada A. Otaify, Samira Esmail, Ola M. Eid, Amal M. Mohamed, Maha S. Zaki, Engy A. Ashaat, Mona Aglan, Ghada El-Kamah, Mona K. Mekkawy, Hanan H. Afifi, Shymaa H Hussein, Inas Mazen, Heba ElAwady, Ghada M H Abdel-Salam
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b91fae0e36b4e8b127f3accb52d3f6e
https://doaj.org/article/2bfe665e28c74ca3b3ab3b493e122b7b
https://doaj.org/article/2bfe665e28c74ca3b3ab3b493e122b7b