HIGHLIGHTS
- who: Bochra Khadija from the Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University have published the research: Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review, in the Journal: (JOURNAL)
- what: The study is based on the analysis of two patients with corpus callosum malformations, which are characterized by genetic and phenotypic heterogeneity.
SUMMARY
Corpus callosum malformations (CCM) represent one of the most common congenital cerebral malformations with a prevalence of around one for . . .
If you want to have access to all the content you need to log in!
Thanks :)
If you don't have an account, you can create one here.