Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290-300
Am J Med Genet A
.
2018 Nov;176(11):2522.
doi: 10.1002/ajmg.a.38846.
Epub 2018 Sep 20.
Authors
C M Clarke
1
,
V T Fok
1
,
J A Gustafson
1
,
M D Smyth
2
3
,
A E Timms
1
,
C D Frazar
4
,
J D Smith
4
,
C B Birgfeld
5
6
7
,
A Lee
7
8
9
,
R G Ellenbogen
7
8
9
,
J S Gruss
5
6
7
,
R A Hopper
5
6
7
,
M L Cunningham
1
7
10
Affiliations
1
Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
2
Washington University Department of Neurosurgery, St. Louis, Missouri.
3
St. Louis Children's Hospital, St. Louis, Missouri.
4
Department of Genome Sciences, University of Washington, Seattle, Washington.
5
Division of Plastic Surgery, Department of Surgery, University of Washington School of Medicine, Seattle, Washington.
6
Division of Craniofacial and Plastic Surgery, Seattle Children's Hospital, Seattle, Washington.
7
Seattle Children's Craniofacial Center, Seattle Children's Hospital, Seattle, Washington.
8
Department of Neurological Surgery, University of Washington School of Medicine, Seattle, Washington.
9
Department of Pediatric Neurosurgery, Seattle Children's Hospital, Seattle, Washington.
10
Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.
PMID:
30537273
DOI:
10.1002/ajmg.a.38846
No abstract available
Publication types
Published Erratum