Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Laila K.E. Effat"'
Autor:
Rania R. Ahmed, Amina M. Medhat, Germine M. Hamdy, Laila K.E. Effat, Mohamed S. Abdel-Hamid, Ghada M.H. Abdel-Salam
Publikováno v:
Molecular Syndromology. :1-10
Introduction: The underlying molecular defects of congenital hydrocephalus are heterogeneous and many isolated forms of hydrocephalus remain unsolved at the molecular level. Congenital hydrocephalus in males associated with agenesis of the corpus cal