Ropers, H. H. Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Cingoz, S., Bache, I., Bjerglund, L., Ropers, H. H., Tommerup, N., Jensen, H., et al. (2011). Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects. Am J Med Genet A, 155A(1), 203-6. Retrieved from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=21204233 http://onlinelibrary.wiley.com/store/10.1002/ajmg.a.33766/asset/33766_ftp.pdf?v=1&t=gywo8iu9&s=11eb1c875f786487e81c141cc7fb4a6d7082c4b8.