Author Index

A

  • Abdallah, Zeinab Y. Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program [Volume 9, Issue 1, 2020]
  • Abd Elazim, Rania A. Effect of interleukin-10 polymorphism on susceptibility to type I diabetes in children with latent toxoplasmosis [Volume 9, Issue 1, 2020]
  • Abdelaziz, Doaa M. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]
  • Abdel-Ghafar, Sherif F. Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Abd El-Ghany, Hoda M. Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation [Volume 9, Issue 2, 2021]
  • Abdel-Hamid, Mohamed S. Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • AbulEzz, Eman A. Orodental abnormalities in limb malformation syndromes: A review article [Volume 9, Issue 1, 2020]
  • Abulnasr, Ahmed L Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Aglan, Mona S. Orodental abnormalities in limb malformation syndromes: A review article [Volume 9, Issue 1, 2020]
  • Aglan, Mona S. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]
  • Aglan, Mona S. Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Ali, Ola S. M. Evaluation of the gene expression in Egyptian patients with familial Mediterranean fever [Volume 9, Issue 2, 2021]
  • Amr, Khalda Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program [Volume 9, Issue 1, 2020]
  • Ashaat, Engy A. Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Awad, Soha I. Effect of interleukin-10 polymorphism on susceptibility to type I diabetes in children with latent toxoplasmosis [Volume 9, Issue 1, 2020]

E

  • Elaidy, Aya Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]
  • El-Badry, Tarek Orodental abnormalities in limb malformation syndromes: A review article [Volume 9, Issue 1, 2020]
  • El-Bassyouni, Hala T. Evaluation of the gene expression in Egyptian patients with familial Mediterranean fever [Volume 9, Issue 2, 2021]
  • Elbeltagy, Nanis S. Effect of interleukin-10 polymorphism on susceptibility to type I diabetes in children with latent toxoplasmosis [Volume 9, Issue 1, 2020]
  • Eldessouky, Sara H. Counseling challenges for prenatal diagnosis [Volume 9, Issue 2, 2021]
  • Elhossini, Rasha Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Elhossini, Rasha M. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]
  • EL-Kamah, Ghada Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program [Volume 9, Issue 1, 2020]

F

  • Fayez, Alaaeldin Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]
  • Fayez, Alaaeldin G. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]

G

  • Ghorab, Raghda M. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]

H

  • Hamed, Eman Effect of interleukin-10 polymorphism on susceptibility to type I diabetes in children with latent toxoplasmosis [Volume 9, Issue 1, 2020]
  • Hammad, Saida A. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]
  • Hassib, Nehal F. Orodental abnormalities in limb malformation syndromes: A review article [Volume 9, Issue 1, 2020]
  • Hussen, Dalia F. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]

I

  • Ibrahim, Ilham Y. Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation [Volume 9, Issue 2, 2021]
  • Ibrahim, Mona Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program [Volume 9, Issue 1, 2020]
  • Ismail, Samira Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]

K

  • Kholoussi, Shams M. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]

L

  • Lotfy, Randa S. Evaluation of the gene expression in Egyptian patients with familial Mediterranean fever [Volume 9, Issue 2, 2021]

M

  • Mamdouh, Rasha M. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]
  • Megahed, Hisham Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Momen, Nouran N. Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation [Volume 9, Issue 2, 2021]

N

  • Nassar, Yasser Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program [Volume 9, Issue 1, 2020]
  • Nosier, Soha S. Quantification of hemoglobin peptides in Beta-thalassemia patients using tandem mass spectrometry for future national screening program [Volume 9, Issue 1, 2020]

O

  • Omar, Lobna A. Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation [Volume 9, Issue 2, 2021]
  • Otaify, Ghada A. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]
  • Otaify, Ghada A. Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]

R

  • Ramzy, Magda Orodental abnormalities in limb malformation syndromes: A review article [Volume 9, Issue 1, 2020]
  • Raouf, Haiam A. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]
  • Refaat, Khaled M. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]

S

  • Samy, Rania M. Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation [Volume 9, Issue 2, 2021]
  • Shehata, Ghada M. Evaluation of the gene expression in Egyptian patients with familial Mediterranean fever [Volume 9, Issue 2, 2021]

T

  • Temtamy, Samia A. Orodental abnormalities in limb malformation syndromes: A review article [Volume 9, Issue 1, 2020]
  • Temtamy, Samia A. Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation [Volume 9, Issue 1, 2020]
  • Temtamy, Samia A. One hundred years since Victor McKusick's birth: a tribute from Greece [Volume 9, Issue 1, 2020]
  • Temtamy, Samia A. Counseling challenges for prenatal diagnosis [Volume 9, Issue 2, 2021]
  • Temtamy, Samia A. Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes in two Egyptian families [Volume 9, Issue 2, 2021]
  • Temtamy, Samia A. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]

Y

  • Yahya, Raida S. Effect of interleukin-10 polymorphism on susceptibility to type I diabetes in children with latent toxoplasmosis [Volume 9, Issue 1, 2020]

Z

  • Zakaria, Nahla M. Immunological profile of patients with skeletal dysplasia and disproportionate short stature [Volume 9, Issue 2, 2021]
  • Zarouk, Waheba A. Evaluation of the gene expression in Egyptian patients with familial Mediterranean fever [Volume 9, Issue 2, 2021]