1. Deletions;Schinzel,2001
2. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1→pter) and partial monosomy 9p (9p22→pter);Chen;Prenat. Diagn.,2005
3. Partial trisomy 1p (1p36.22→pter) and partial monosomy 9p (9p22.2→pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl;Chen;Genet. Couns.,2006
4. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwan;Chen;J. Obstet. Gynecol.,2011
5. Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly;Chen;Genet. Couns.,2012