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DDU144
DDU144
http://dx.doi.org/10.1093/HMG/DDU144
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P356
Q38308028-07B3A8E8-EE52-476F-8A92-D11830A0FE13
P356
DDU144
http://dx.doi.org/10.1093/HMG/DDU144