Disease: Mesomelic syndrome Pfeiffer type
- A variant of Reinhardt-Pfeiffer mesomelic skeletal dysplasia
- Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes at 8q13
- Mesomelic dysplasia with acral synostoses Verloes-David-Pfeiffer type: follow-up study documents progressive clinical course
- Reinhardt-Pfeiffer mesomelic dysplasia or dyschondrosteosis? Is the distinction well-founded? Apropos of a familial case with variable expression
- Study of the classification of chondrodysplasias with mesomelic predominance