Journal: American Journal of Human Genetics
Article Title: Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations
doi: 10.1016/j.ajhg.2009.05.005
Figure Lengend Snippet: Array CGH-Detected Microdeletions in 16q24
Article Snippet: Chromosomal microarray analysis was performed with the use of the V6.1 BAC-based array (patient D4), V6.3 OLIGO (patients D5 and D7), and V7.2 OLIGO (patient D3), designed by Baylor Medical Genetics laboratories and manufactured by Agilent Technology as previously described., Array CGH in patient D5 was performed with the use of the BAC clone SignatureChipWG whole-genome microarray, in patient D6 with the use of the SignatureChipOS, a 105K-feature whole-genome microarray (made for Signature Genomic Laboratories by Agilent Technologies), in accordance with the manufacturer's instructions.
Techniques: