• 19q13.33→qter trisomy in a girl with intellectual impairment and seizures
• A case of mosaic trisomy 19q12-q13.2 with high BMI, macrocephaly, and speech delay: does USF2 determine size in the 19q phenotypes?
• A Novel 1.13 Mb Interstitial Duplication at 19q13.32 Causing Developmental Delay and Microcephaly in a Pediatric Patient: the First Asian Case Reports
• De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly
• Direct tandem duplication in chromosome 19q characterized by array CGH
• Duplication of 19q (13.2-13.31) associated with comitant esotropia: A case report
• Familial subtelomeric rearrangement of chromosomes 19 and 20: a new contribution to partial distal 19q trisomy
• First-line temozolomide chemotherapy in progressive low-grade astrocytomas after radiotherapy: molecular characteristics in relation to response
• Loss of heterozygosity at 1p-19q induces a global change in oligodendroglial tumor gene expression
• Partial duplication of chromosome 19 associated with syndromic duane retraction syndrome
• Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay
• Prenatal diagnosis of complete trisomy 19q
• Proximal 19q trisomy: a new syndrome of morbid obesity and mental retardation
• Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring
• Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation