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

Autor: Mohamed, Amal M.1 (AUTHOR) amalmahmoud15@yahoo.com, Kamel, Alaa K.1 (AUTHOR), Eid, Maha M.1 (AUTHOR), Eid, Ola M.1 (AUTHOR), Mekkawy, Mona1 (AUTHOR), Hussein, Shymaa H.1 (AUTHOR), Zaki, Maha S.2 (AUTHOR), Esmail, Samira2 (AUTHOR), Afifi, Hanan H.2 (AUTHOR), El‐Kamah, Ghada Y.2 (AUTHOR), Otaify, Ghada A.2 (AUTHOR), El‐Awady, Heba Ahmed3 (AUTHOR), Elaidy, Aya2 (AUTHOR), Essa, Mahmoud Y.2 (AUTHOR), El‐Ruby, Mona2 (AUTHOR), Ashaat, Engy A.2 (AUTHOR), Hammad, Saida A.1 (AUTHOR), Mazen, Inas2 (AUTHOR), Abdel‐Salam, Ghada M. H.2 (AUTHOR), Aglan, Mona2 (AUTHOR)
Zdroj: Molecular Genetics & Genomic Medicine. Nov2021, Vol. 9 Issue 11, p1-15. 15p.
Databáze: Academic Search Ultimate