Defining the molecular pathology and consequent phenotypes in Egyptian HB patients

por El-Kamah, Ghada Y., Mosaad, Rehab M., Taher, Mohamed B., Amr, Khalda S.
Publicado 2021

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families

por El-Kamah, Ghada Y., Mehrez, Mennat I., Taher, Mohamed B., El-Bassyouni, Hala T., Gaber, Khaled R., Amr, Khalda S.
Publicado 2023

Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children

por Eissa, Eman, Afifi, Hanan H., Abo-Shanab, Assem M., Thomas, Manal M., Taher, Mohamed B., Kandil, Rania, Kholoussi, Naglaa M.
Publicado 2023

Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients

por Sokkar, Mona F., Hamdy, Mona, Erian, Peter SF, Mosaad, Rehab M., Elaraby, Nesma M., Taher, Mohamed B., El-Sayed, Heba, Al Komy, Mohammed, Eid, Maha M., Mohamed, Amal M., Amr, Khalda S., El-Kamah, Ghada Y.
Publicado 2023