• 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 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47,XYY) with syndactyly, type III Waardenburg syndrome, and congenital heart disease
• A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability
• A novel chromosome 2q24.3-q32.1 microdeletion in a fetus with multiple malformations
• A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations
• A novel interstitial deletion of chromosome 2q21.1-q23.3: Case report and literature review
• Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q
• Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2q
• Microdeletion 2q23.3q24.1: exploring genotype-phenotype correlations
• Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis
• Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency
• Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p
• Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement
• Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
• Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes
• Reorganization of <em>inter-</em>chromosomal interactions in the 2q37-deletion syndrome
• Subtelomeric fish findings in Turkish patients with idiopathic mental retardation
• Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study