Author Index

A

  • Abdel Baky, Olweya M. Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]
  • Abd El-Ghany, Hoda M. Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation [Volume 7, Issue 2, 2018]
  • Abdel Raouf, Sahar M. Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders [Volume 7, Issue 2, 2018]
  • Aboul-Ezz, Eman H. A. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • Adebisi, Samuel S. MicroRNA-mediated sensitization of lung cancer cells to chemotherapeutics: the roles of miR-21 and miR-155 [Volume 7, Issue 2, 2018]
  • Aglan, Mona S. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]
  • Al-Gamal, Rasha A. Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation [Volume 7, Issue 2, 2018]
  • Amin, Sherine K. Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]
  • Ashaat, Engy A. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]

D

  • Danborno, Barnabas MicroRNA-mediated sensitization of lung cancer cells to chemotherapeutics: the roles of miR-21 and miR-155 [Volume 7, Issue 2, 2018]

E

  • Ehssan, Eman A. Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation [Volume 7, Issue 2, 2018]
  • El-Awady, Heba Assessment of serum level of vitamin D in infants and children with Down syndrome [Volume 7, Issue 2, 2018]
  • Elbagoury, Nagham M. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]
  • El-Bagoury, Nagham M. Genome-editing technologies: Advancement, clinical applications, and ethical concerns [Volume 7, Issue 2, 2018]
  • El-Bassyouni, Hala T. Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders [Volume 7, Issue 2, 2018]
  • El-Deen, Amany S. Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation [Volume 7, Issue 2, 2018]
  • El-Deen, Menatalla K. Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation [Volume 7, Issue 2, 2018]
  • El-Hawary, Manal M. Assessment of serum level of vitamin D in infants and children with Down syndrome [Volume 7, Issue 2, 2018]
  • El Ruby, Mona O. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • El Ruby, Mona O. Updates about ethical, legal and psychological implications of genetic testing in newborns, children and adolescents [Volume 7, Issue 2, 2018]
  • El Ruby, Mona O. Genetic syndromes with immunological disturbances [Volume 7, Issue 2, 2018]
  • El-Shafie, Shahira M Assessment of serum level of vitamin D in infants and children with Down syndrome [Volume 7, Issue 2, 2018]
  • El-Shoubary, Alia M. Genetic study of the association of specific language impairment to markers near gene [Volume 7, Issue 2, 2018]
  • Essawi, Mona L. Genetic study of the association of specific language impairment to markers near gene [Volume 7, Issue 2, 2018]
  • Essawi, Mona L. Genome-editing technologies: Advancement, clinical applications, and ethical concerns [Volume 7, Issue 2, 2018]
  • Essawi, Mona L. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]

F

  • Farag, Mona K. Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders [Volume 7, Issue 2, 2018]
  • Fateen, Ekram M. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]

G

  • Gaber, Khaled R. Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders [Volume 7, Issue 2, 2018]

H

  • Hammad, Saida A. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • Hassan, Heba A. Genome-editing technologies: Advancement, clinical applications, and ethical concerns [Volume 7, Issue 2, 2018]
  • Helmy, Nivine Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]

I

  • Ibrahim, Mona M. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]
  • Ismail, Samira Genetic study of the association of specific language impairment to markers near gene [Volume 7, Issue 2, 2018]
  • Ismail, Samira Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • Ismail, Samira Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]
  • Issa, Mahmoud Y. Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]

K

  • Kamel, Alaa K. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • Kamel, Alaa K. Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]
  • Khattab, Ahmed N. Genetic study of the association of specific language impairment to markers near gene [Volume 7, Issue 2, 2018]

M

  • Mohamed, Amal M. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]

N

  • Nabile, Raooth Assessment of serum level of vitamin D in infants and children with Down syndrome [Volume 7, Issue 2, 2018]
  • Nawito, Wasela M. Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders [Volume 7, Issue 2, 2018]
  • Ndodo, Nnaemeka D. MicroRNA-mediated sensitization of lung cancer cells to chemotherapeutics: the roles of miR-21 and miR-155 [Volume 7, Issue 2, 2018]

R

  • Ragab, Tamer Assessment of serum level of vitamin D in infants and children with Down syndrome [Volume 7, Issue 2, 2018]

S

  • Salman, Tarek M. Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders [Volume 7, Issue 2, 2018]
  • Samy, Rania M. Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation [Volume 7, Issue 2, 2018]
  • Sayed, Inas S. M. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • Sayed, Ola M. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]
  • Sayed-Ahmed, Mohammed M. Genetic study of the association of specific language impairment to markers near gene [Volume 7, Issue 2, 2018]
  • Sharaf-Eldin, Wessam E. Genome-editing technologies: Advancement, clinical applications, and ethical concerns [Volume 7, Issue 2, 2018]
  • Soliman, Hala N. Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder [Volume 7, Issue 2, 2018]

Z

  • Zaki, Maha S. Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 [Volume 7, Issue 2, 2018]
  • Zaki, Maha S. Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies [Volume 7, Issue 2, 2018]
  • Zaki, Moushira E. Genetic study of the association of specific language impairment to markers near gene [Volume 7, Issue 2, 2018]