3′ UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay

Keyphrases

• 3′-untranslated Region (3′-UTR) 100%
• Developmental Delay 100%
• Brain Abnormalities 100%
• FBXO28 100%
• SNP 66%
• Microarray Analysis 66%
• Oligonucleotide Array 66%
• Intellectual Disability 33%
• Microarray 33%
• Seizure 33%
• New Evidence 33%
• Clinical Phenotype 33%
• Clinical Features 33%
• Copy number Variation 33%
• Genome Analysis 33%
• Critical Genes 33%
• Dysmorphology 33%
• Functional Importance 33%
• Phenotypic Spectrum 33%
• Microdeletion Syndrome 33%
• Potential Functional 33%
• Reporting Criteria 33%
• Developmental Brain 33%
• 1q41q42 33%

Biochemistry, Genetics and Molecular Biology

• Single Nucleotide Polymorphism 100%
• Oligonucleotide Microarrays 100%
• Karyotype 50%
• Exome Sequencing 50%
• Intellectual Disability 50%
• Microdeletion Syndrome 50%