Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation

Keyphrases

• Clinical Characterization 100%
• Microdeletion 100%
• Molecular Characterization 100%
• Mild Mental Retardation 100%
• Copy number Variation 33%
• Generalized Seizures 33%
• Neuronal Development 33%
• Microcephaly 33%
• Pathogenicity 33%
• Mild Dysmorphic Features 33%
• Molecular Karyotyping 33%
• Language Development 33%
• Sensorineural Hearing Loss 33%

Biochemistry, Genetics and Molecular Biology

• Chromosome 100%
• Copy-Number Variation 50%
• Karyotyping 50%
• Language Development 50%
• Hearing 50%