Volume & Issue: Volume 7, Issue 2, July 2018 
Assessment of serum level of vitamin D in infants and children with Down syndrome

Manal M. El-Hawary; Shahira M El-Shafie; Heba El-Awady; Tamer Ragab; Raooth Nabile


Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders

Hala T. El-Bassyouni; Sahar M. Abdel Raouf; Mona K. Farag; Wasela M. Nawito; Tarek M. Salman; Khaled R. Gaber


Genetic study of the association of specific language impairment to markers near gene

Mohammed M. Sayed-Ahmed; Samira Ismail; Alia M. El-Shoubary; Mona L. Essawi; Moushira E. Zaki; Ahmed N. Khattab


Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation

Hoda M. Abd El-Ghany; Eman A. Ehssan; Menatalla K. El-Deen; Rasha A. Al-Gamal; Rania M. Samy; Amany S. El-Deen


Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22

Samira Ismail; Alaa K. Kamel; Engy A. Ashaat; Amal M. Mohamed; Maha S. Zaki; Eman H. A. Aboul-Ezz; Saida A. Hammad; Inas S. M. Sayed; Mona O. El Ruby


Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies

Mahmoud Y. Issa; Samira Ismail; Nivine Helmy; Alaa K. Kamel; Sherine K. Amin; Olweya M. Abdel Baky; Maha S. Zaki


Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder

Mona L. Essawi; Nagham M. Elbagoury; Ola M. Sayed; Mona S. Aglan; Mona M. Ibrahim; Hala N. Soliman; Ekram M. Fateen