EKB Journal Management System
Volume & Issue: Volume 10, Issue 2, June 2022  XML
1

Autism spectrum disorder and achondroplasia in an Egyptian patient

Samira Ismail; Hisham Megahed; Somaya Ismail; Amina Hindawy
2

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

Srivathsa T. Reddy
3

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

Srivathsa T. Reddy
4

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
5

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
6

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
7

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