Untangling Sources of Phenotypic Variation Characterizing the Craniofacial Disease Holoprosencephaly Article

Lainoff, Alexis, Young, Nathan, Hallgrimsson, Benedikt et al. (2018). Untangling Sources of Phenotypic Variation Characterizing the Craniofacial Disease Holoprosencephaly . FASEB JOURNAL, 32(S1), 776.11-776.11. 10.1096/fasebj.2018.32.1_supplement.776.11

cited authors

  • Lainoff, Alexis; Young, Nathan; Hallgrimsson, Benedikt; Marcucio, Ralph

authors

publication date

  • April 1, 2018

published in

keywords

  • 31 Biological Sciences
  • 32 Biomedical and Clinical Sciences
  • 3202 Clinical Sciences
  • Brain Disorders
  • Dental/Oral and Craniofacial Disease
  • Genetics
  • Pediatric Research Initiative
  • Rare Diseases

publisher

  • Wiley

start page

  • 776.11

end page

  • 776.11

volume

  • 32

issue

  • S1