GATAD2B Gene microdeletion causing intellectual disability autosomal dominant type 18: Case report and review of the literature

Medicine and Dentistry

• Autosomal Dominant Inheritance 100%
• Array Comparative Genomic Hybridization 100%
• Molecular Diagnosis 50%
• Pervasive Developmental Disorder 50%
• Genomic Instability 50%
• Exon 50%
• Dysmorphic Feature 50%
• Haploinsufficiency 50%
• Fatty Acid Transporter 50%
• Patient with Intellectual Disability 50%
• Genotype Phenotype Correlation 50%
• Thumb 50%
• Hypotrophy 50%
• Language Delay 50%
• Genetic Counseling 50%
• Mental Instability 50%

Biochemistry, Genetics and Molecular Biology

• Genotype-Phenotype Correlation 33%