Two locus inheritance of non-syndromic midline craniosynostosis via rare

Authors

Andrew T Timberlake
Jungmin Choi
Samir Zaidi
Qiongshi Lu
Carol Nelson-Williams
Eric D Brooks
Kaya Bilguvar
Irina Tikhonova
Shrikant Mane
Jenny F Yang
Rajendra Sawh-Martinez
Sarah Persing
Elizabeth G Zellner
Erin Loring
Carolyn Chuang
Amy Galm
Peter W Hashim
Derek M Steinbacher
Michael L DiLuna
Charles C Duncan
Kevin A Pelphrey, George Washington University
Hongyu Zhao
John A Persing
Richard P Lifton

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