Two locus inheritance of non-syndromic midline craniosynostosis via rare
Document Type
Journal Article
Publication Date
9-8-2016
Journal
Elife
Volume
5
DOI
10.7554/eLife.20125
Keywords
Alleles; Bone Morphogenetic Protein 2; Craniosynostoses; Exome; Genetic Association Studies; Humans; Infant; Mutation; Penetrance; Sequence Analysis, DNA; Smad6 Protein
APA Citation
Timberlake, A., Choi, J., Zaidi, S., Lu, Q., Nelson-Williams, C., Brooks, E., Bilguvar, K., Tikhonova, I., Mane, S., Yang, J., Sawh-Martinez, R., Persing, S., Zellner, E., Loring, E., Chuang, C., Galm, A., Hashim, P., Steinbacher, D., DiLuna, M., Duncan, C., Pelphrey, K., Zhao, H., Persing, J., & Lifton, R. (2016). Two locus inheritance of non-syndromic midline craniosynostosis via rare. Elife, 5 (). http://dx.doi.org/10.7554/eLife.20125
Peer Reviewed
1
