bibliographic resource 2385662 [br/2385662]
https://w3id.org/oc/corpus/br/2385662

is a
title
  • Exome sequencing identifiesDYNC2H1mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
publication date
  • 2013-01-01
contributor
format
identifier
part of