Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1
Abdel‐Aziz, Nahla, El‐Kamah, Ghada, Khairat, Rabab, Mohamed, Hanan, Gad, Yehia, El‐Ghor, Akmal M., Amr, Khalda S.
Published in Molecular genetics & genomic medicine (01.12.2021)
Published in Molecular genetics & genomic medicine (01.12.2021)
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Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly
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
Published in Molecular genetics & genomic medicine (01.11.2021)
Published in Molecular genetics & genomic medicine (01.11.2021)
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Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75]
El-Kamah, Ghada Y., Mosaad, Rehab M., Taher, Mohamed B., Amr, Khalda S.
Published in Journal of Genetic Engineering and Biotechnology (01.06.2024)
Published in Journal of Genetic Engineering and Biotechnology (01.06.2024)
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Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families
El-Kamah, Ghada Y, Mehrez, Mennat I, Taher, Mohamed B, El-Bassyouni, Hala T, Gaber, Khaled R, Amr, Khalda S
Published in Genes (12.04.2023)
Published in Genes (12.04.2023)
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Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities
Elhadidi, Sahar Mostafa, Hassan, Mohamed Ossama, Soliman, Nadia Lashin, Abouel-Ezz, Eman Hassan, ElBatran, Mona Mahmoud, El-Kamah, Ghada Y., Amr, Khalda Sayed
Published in Bulletin of the National Research Centre (01.12.2024)
Published in Bulletin of the National Research Centre (01.12.2024)
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Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease
Sayed Amr, Khalda, El-Bassyouni, Hala T, Abdel Hady, Sawsan, Mostafa, Mostafa I, Mehrez, Mennat I, Coviello, Domenico, El-Kamah, Ghada Y
Published in Genes (29.09.2021)
Published in Genes (29.09.2021)
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Gene Mutations of the Three Ectodysplasin Pathway Key Players ( EDA , EDAR , and EDARADD ) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
Ahmed, Hoda A, El-Kamah, Ghada Y, Rabie, Eman, Mostafa, Mostafa I, Abouzaid, Maha R, Hassib, Nehal F, Mehrez, Mennat I, Abdel-Kader, Mohamed A, Mohsen, Yasmine H, Zada, Suher K, Amr, Khalda S, Sayed, Inas S M
Published in Genes (08.09.2021)
Published in Genes (08.09.2021)
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Ligneous Conjunctivitis with Oral Mucous Membrane Involvement and Decreased Plasminogen Level
El‐Darouti, Mohamed, Zayed, Amira A., El‐Kamah, Ghada Y., Mostafa, Mostafa I.
Published in Pediatric dermatology (01.07.2009)
Published in Pediatric dermatology (01.07.2009)
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A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder
Abdel‐Salam, Ghada M.H., Miyake, Noriko, Eid, Maha M., Abdel‐Hamid, Mohamed S., Hassan, Nihal A., Eid, Ola M., Effat, Laila K., El‐Badry, Tarek H., El‐Kamah, Ghada Y., El‐Darouti, Mohamed, Matsumoto, Naomichi
Published in American journal of medical genetics. Part A (01.11.2011)
Published in American journal of medical genetics. Part A (01.11.2011)
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Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients
Sokkar, Mona F, Hamdy, Mona, Taher, Mohamed B, El-Sayed, Heba, Bayomi, Eman Abdelmotaleb, Amr, Khalda S, El-Kamah, Ghada Y
Published in Biochemical genetics (02.07.2024)
Published in Biochemical genetics (02.07.2024)
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Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt
El-Kamah, Ghada Y, Mohamed, Amal M, Gad, Yehia Z, Abdelhak, Sonia, Hennig, Branwen J, Ramesar, Raj S, Landouré, Guida, Gaye, Amadou, Newport, Melanie J, Williams, Scott M, Ramsay, Michèle
Published in The American journal of tropical medicine and hygiene (01.04.2020)
Published in The American journal of tropical medicine and hygiene (01.04.2020)
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Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients
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.
Published in Journal of Genetic Engineering and Biotechnology (01.12.2023)
Published in Journal of Genetic Engineering and Biotechnology (01.12.2023)
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Lipoid proteinosis: A clinical and molecular study in Egyptian patients
Afifi, Hanan H., Amr, Khalda S., Tosson, Angie M.S., Hassan, Tarak A., Mehrez, Mennat I., El-Kamah, Ghada Y.
Published in Gene (10.09.2017)
Published in Gene (10.09.2017)
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Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant
Afifi, Hanan H., El-Kamah, Ghada Y., Kamel, Alaa K., Abd Allah, Sally G., Hammad, Sayda, Sayed-Ahmed, Mohammed M., Hussein, Shymaa H., Mohamed, Amal M.
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.06.2021)
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.06.2021)
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Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia
Eid, Maha M., Abdel-Messih, Ibrahim Y., El-Kamah, Ghada Y., Mahmoud, Hanan M., Shihab, Marwa I., El-Azhary, Nermeen H.
Published in Middle East Journal of Medical Genetics (01.01.2015)
Published in Middle East Journal of Medical Genetics (01.01.2015)
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Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients
Salem, Ahmed M., El-Bassyouni, Hala T., El-Kamah, Ghada Y., Zarouk, Waheba A., Eid, Maha M., Mosaad, Rehab M., Sayed, Ahmed A., Temtamy, Samia A.
Published in Middle East Journal of Medical Genetics (01.01.2014)
Published in Middle East Journal of Medical Genetics (01.01.2014)
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Outlining the Clinical Profile of ITCIRG1 14 Variants/I including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families
El-Kamah, Ghada Y, Mehrez, Mennat I, Taher, Mohamed B, El-Bassyouni, Hala T, Gaber, Khaled R, Amr, Khalda S
Published in Genes (01.04.2023)
Published in Genes (01.04.2023)
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