Volume & Issue: Volume 8, Issue 2, July 2020 
| 1 | Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification | |
| Mennat I. Mehrez; Nehal Hassib; Inas Sayed; Eman Aboul-Ezz; Magda I. Ramzy; Saher M. El-Hadidi; Mohmed Abdel-Kader; Nermeen El Moataz Bellah; Mona Aglan; Samira Ismail; Laila Hosny; Ghada Otaify; Rasha El-Husseini; Asmaa M. Esmail; Dina El-Desouky; Samia A. Temtamy | ||
| 2 | A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus | |
| Aliaa A. El-Fattha; Amira A. AbdelAzeem; Ahmed A. Zaki; Moushira E. Zaki; Ismail A. Abdelhamid; Somaia M. Ismail | ||
| 3 | Biochemical diagnosis of Wolman disease among patients with suspected lysosomal storage diseases | |
| Ekram Fateen; Mohammed Akmal El Ghor; Marwa Bahaa El Deen Deen Dakroury | ||
| 4 | Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease | |
| Ekram M. Fateen; Heba M. Fathy; Abeer I. Abd El-Fattah; Hala N. Soliman; Nagham M. Elbagoury; Mona L. Essawi | ||
| 5 | A rare mutation in an Egyptian family with Sanfilippo B syndrome | |
| Eman E. A. Mohammed; Ekram M. Fateen | ||
| 6 | Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study | |
| Shaimaa S. Ammar; Heba S. Kassem; Hoda H. Alassi; Shaimaa A. Anwar | ||
| 7 | Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion | |
| Assad M. S. Elgerzawy; Alaa K. Kamel; Mona O. El Ruby; Sayda Hammad; Engy A. Ashaat; Shymaa H. Hussein; Saly G. Abd Allah; Ola M. Eid; Amal M. Mohamed | ||
| 8 | Cytogenetic study of a large cohort of patients with corpus callosum abnormalities | |
| Dalia F. Hussen; Alaa K. Kamel; Mona Mekkawy; Amal M. Mohamed; Maha S. Zaki; Mahmoud Y. Issa; Mona O. El Ruby; Engy A. Ashaat; Samira Ismail; Khaled M. Refaat; Nivine A. Helmy | ||
| 9 | Bone-specific therapeutic modalities for genetic skeletal diseases | |
| Samia A. Temtamy | ||
| 10 | A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa | |
| Ghada El-Kamah; Lamia Mansour; Enas Mahmoud; Mohamed El Darouti; Hoda Radwan; Khalda Amr | ||
| 11 | Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity | |
| Naglaa Kholoussi; Shams Kholoussi; Hala T. El-Bassyouni; Haiam A. Raouf; Iman Helwa; Mohamed I. Gadelhak; Ghada N. Eldeen; Hala Elnady | ||
| 12 | A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management | |
| Nehal F. Hassib; Mohamed A. AbdelKader; Eman A. AbulEzz; Mona S. Aglan; Samia A. Temtamy | ||
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