• 2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotonia
• 2q24 deletions: further characterization of clinical findings and their relation to the SCN cluster
• A 2q24.2 microdeletion containing TANK as novel candidate gene for intellectual disability
• A 2q24.3q31.1 microdeletion found in a patient with Filippi-like syndrome phenotype: a case report
• A case of West syndrome with a deletion at chromosome 2q24.3-q31.3
• A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl
• A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14
• A novel chromosome 2q24.3-q32.1 microdeletion in a fetus with multiple malformations
• CCDD Phenotype Associated with a Small Chromosome 2 Deletion
• De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia
• Hearing impairment in a female infant with interstitial deletion of 2q24.1q24.3
• Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures
• Interstitial deletion of 2q24.2: further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction
• Possible genes responsible for developmental delay observed in patients with rare 2q23q24 microdeletion syndrome: Literature review and description of an additional patient
• Severe pulmonary emphysema in a girl with interstitial deletion of 2q24.2q24.3 including ITGB6