Short Communication6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay
Keywords: LAC; aCGH; array comparative genomic hybridization; OMIM; Online Mendelian Inheritance in Man; CCD; cleidocranial dysplasia; QF-PCR; quantitative fluorescent polymerase chain reaction; BAC; bacterial artificial chromosome; FISH; fluorescence in situ hybridizat