Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome

Keyphrases

• Phenotypic Characteristics 100%
• Analytic Approach 100%
• Trigonocephaly 100%
• Chromosome 9p Deletion Syndrome 100%
• FREM1 66%
• Non-overlapping Regions 66%
• Psychiatric Diagnosis 33%
• Atopic Disease 33%
• Whole Genome Sequencing 33%
• Large Cohort 33%
• Medical Records 33%
• Genotype 33%
• Gastroesophageal Reflux Disease 33%
• High-resolution 33%
• Congenital Heart Disease 33%
• Regulatory Elements 33%
• Caregivers 33%
• Region-based Analysis 33%
• Autism Spectrum Disorder 33%
• Hypotonia 33%
• Vision Loss 33%
• Previous Literature 33%
• Genomic Regions 33%
• Dysmorphic Features 33%
• Long Distance 33%
• Functional Constipation 33%
• Neonatal Hypoglycemia 33%
• Guided Interview 33%
• Intellectual Developmental Disorder 33%
• Genotype Data 33%
• Phenotype Data 33%
• Phenotypic Information 33%
• Genital Defects 33%
• New Analytic Method 33%

Biochemistry, Genetics and Molecular Biology

• Genotyping 100%
• Chromosome 9p 100%
• Whole Genome Sequencing 50%
• Medical Record 50%
• Regulatory Element 50%
• Intellectual Disability 50%
• Genomics 50%