Disease: Chromosome 17- deletion 17q23 q24
- 17q23.3 de novo microdeletion involving only TANC2 gene: A new case
- Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha
- Genomic markers for ovarian cancer at chromosomes 1, 8 and 17 revealed by array CGH analysis
- Genomic structure of karyopherin alpha2 ( KPNA2) within a low-copy repeat on chromosome 17q23-q24 and mutation analysis in patients with Russell-Silver syndrome
- Molecular and clinical delineation of the 17q22 microdeletion phenotype