Showing 1 - 8 results of 8 for search 'Ghada Y. El-Kamah', query time: 0.04s Refine Results
  1. 1
    Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75]

    Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75] by Ghada Y. El-Kamah, Rehab M. Mosaad, Mohamed B. Taher, Khalda S. Amr

    Published 2024-06-01
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  2. 2
    Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients

    Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients by Rehab M. Mosaad, Khalda S. Amr, Eman A. Rabie, Naglaa O. Mostafa, Sonia A. Habib, Ghada Y. El‐Kamah

    Published 2021-02-01
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  3. 3
    Outlining the Clinical Profile of <i>TCIRG1 14 Variants</i> including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families

    Outlining the Clinical Profile of <i>TCIRG1 14 Variants</i> including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families by Ghada Y. El-Kamah, Mennat I. Mehrez, Mohamed B. Taher, Hala T. El-Bassyouni, Khaled R. Gaber, Khalda S. Amr

    Published 2023-04-01
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  4. 4
    Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease

    Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease by Khalda Sayed Amr, Hala T. El-Bassyouni, Sawsan Abdel Hady, Mostafa I. Mostafa, Mennat I. Mehrez, Domenico Coviello, Ghada Y. El-Kamah

    Published 2021-09-01
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  5. 5
    Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1

    Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 by Nahla N.Abdel‐Aziz, Ghada Y.El‐Kamah, Rabab A.Khairat, Hanan R.Mohamed, Yehia Z.Gad, Akmal M. El‐Ghor, Khalda S. Amr

    Published 2021-12-01
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  6. 6
    Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities

    Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities by Sahar Mostafa Elhadidi, Mohamed Ossama Hassan, Nadia Lashin Soliman, Eman Hassan Abouel-Ezz, Mona Mahmoud ElBatran, Ghada Y. El-Kamah, Khalda Sayed Amr

    Published 2024-03-01
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  7. 7
    Gene Mutations of the Three Ectodysplasin Pathway Key Players (<i>EDA</i>, <i>EDAR</i>, and <i>EDARADD</i>) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations

    Gene Mutations of the Three Ectodysplasin Pathway Key Players (<i>EDA</i>, <i>EDAR</i>, and <i>EDARADD</i>) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of... by Hoda A. Ahmed, Ghada Y. El-Kamah, Eman Rabie, Mostafa I. Mostafa, Maha R. Abouzaid, Nehal F. Hassib, Mennat I. Mehrez, Mohamed A. Abdel-Kader, Yasmine H. Mohsen, Suher K. Zada, Khalda S. Amr, Inas S. M. Sayed

    Published 2021-09-01
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  8. 8
    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 by 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

    Published 2021-11-01
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