|1.||David, Albert: 2 articles (07/2010 - 10/2009)|
|2.||Isidor, Bertrand: 2 articles (07/2010 - 10/2009)|
|3.||Mortier, Geert R: 2 articles (07/2010 - 10/2009)|
|4.||Verloes, Alain: 2 articles (07/2010 - 10/2009)|
|5.||Leroy, Jules G: 2 articles (07/2010 - 10/2009)|
|6.||Hamel, Antoine: 2 articles (07/2010 - 10/2009)|
|7.||Dawson, Paul A: 1 article (08/2011)|
|8.||Pichon, Olivier: 1 article (07/2010)|
|9.||Kjellén, Lena: 1 article (07/2010)|
|10.||Rauch, Anita: 1 article (07/2010)|
07/09/2010 - "Mesomelia-synostoses syndrome (MSS) or mesomelic dysplasia with acral synostoses Verloes-David-Pfeiffer type is a rare autosomal-dominant disorder characterized by mesomelic limb shortening, acral synostoses, and multiple congenital malformations. "
10/01/2009 - "Verloes-David-Pfeiffer mesomelia-synostoses syndrome is an autosomal-dominant form of mesomelic dysplasia comprising typical acral synostoses combined with ptosis, hypertelorism, palatal abnormality, CHD, and ureteral anomalies. "
|3.||Chondrodysplasia Punctata (Stippled Epiphyses)
08/01/2011 - "The removal of sulfate via sulfatases is an important step in proteoglycan degradation, and defects in several sulfatases are linked to perturbed fetal bone development, including mesomelia-synostoses syndrome and chondrodysplasia punctata 1. In recent years, interest in sulfate and its role in developmental biology has expanded following the characterisation of sulfate transporters, sulfotransferases and sulfatases and their involvement in fetal growth. "