Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms

E-ISSN： 1552-4833|176|2|290-300

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.176, Iss.2, 2018-02, pp. : 290-300

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Heterozygous mutations in ERF cause syndromic craniosynostosis with multiple suture involvement

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2544-2547

John Wiley & Sons Inc

Access to resources Recommend Favorite

Craniosynostosis: Genes and Mechanisms

By Wilkie Andrew O. M.

Human Molecular Genetics, Vol. 6, Iss. 10, 1997-01 ,pp. : 1647-1656

Oxford University Press

Access to resources Recommend Favorite

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

By Mohapatra Bhagyalaxmi Casey Brett Li Hua Ho-Dawson Trang Smith Liana Fernbach Susan D. Molinari Laura Niesh Stephen R. Jefferies John Lynn Craigen William J. Towbin Jeffrey A. Belmont John W. Ware Stephanie M.

Human Molecular Genetics, Vol. 18, Iss. 5, 2009-03 ,pp. : 861-871

Oxford University Press

Access to resources Recommend Favorite

Identification of Rare Variants from Exome Sequence in a Large Pedigree with Autism

Human Heredity, Vol. 74, Iss. 3-4, 2013-04 ,pp. : 153-164

Karger

Access to resources Recommend Favorite

Using Gene Genealogies to Detect Rare Variants Associated with Complex Traits

Human Heredity, Vol. 78, Iss. 3-4, 2014-08 ,pp. : 117-130

Karger

Access to resources Recommend Favorite