Middle East Journal of Medical Genetics

Volume & Issue: Volume 10, Issue 2, June 2022

Autism spectrum disorder and achondroplasia in an Egyptian patient

Samira Ismail; Hisham Megahed; Somaya Ismail; Amina Hindawy

Professor Samia Temtamy: the founder of human genetics at the National Research Centre, Egypt

Srivathsa T. Reddy

Molecular and cytogenetic diagnosis of disorders/differences of sex development: molecular update of genes controlling sexual differentiation

Srivathsa T. Reddy

Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene: expansion in clinical features

Rabab Khairat; Maha S. Zaki; Ahmed I. Harkan; Heba Dawoud

Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders

Haiam A. Raouf; Naglaa Kholoussi; Shams Kholoussi; Botros Morcos; Engy A. Ashaat; Iman Helwa

Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment

Zeinab Y. Abdallah; Soha S. Nosier; Neveen A. Soliman; Ekram Fateen

Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study

Mostafa I. Mostafa; Mohamed A. Abdelkader; Moustapha A. Abdelrahman; Nehal F. Hassib; Inas S. MostafaSayed; Nermeen El.Moataz B. Ahmed; Maha I. Abdelfattah; Mennatahllah I. Mehrez; Yasmin M. Khalil; Tarek H. El-Badry; Maha R. Abouzaid

Journal Archive

Volume 13 (2024)

Volume 12 (2023)

Volume 11 (2022)

Volume 10 (2021)

Issue 2

Issue 1

Volume 9 (2020)

Volume 8 (2019)

Volume 7 (2018)