Fluorescence In SITU Hybridization and Single Nucleotide Polymorphism of A New Case with INV DUP DEP(8p)
Transmitted duplication of 8p23.1–8p23.2 associated with speech delay, autism and learning difficulties
Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event
Inverted duplication/deletion of the short arm of chromosome 8 in two patients with tetralogy of Fallot
Clinical and Cytogenetic Findings in Seven Cases of Inverted Duplication of 8p With Evidence of a Telomeric Deletion Using Fluorescence in Situ Hybridization
