Related Articles

• DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets
• A novel method to detect the Mexican founder mutation BRCA1 ex9‑12del associated with breast and ovarian cancer using quantitative polymerase chain reaction and TaqMan® probes
• Smith‑Magenis syndrome in monozygotic twin fetuses presenting with discordant phenotypes and uteroplacental insufficiency
• Identification of a 0.4 Kb deletion region in 10q26 associated with endometrial carcinoma
• High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH