Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis
Titel:
Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis
Auteur:
Smith, Joshua D. Hing, Anne V. Clarke, Christine M. Johnson, Nathan M. Perez, Francisco A. Park, Sarah S. Horst, Jeremy A. Mecham, Brig Maves, Lisa Nickerson, Deborah A. Cunningham, Michael L.