Whole‐exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways-Reference-Cited by-同舟云学术

Whole‐exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways

Published:2022-01-25 Issue:5 Volume:188 Page:1464-1475
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Tønne Elin¹²³^ORCID,Due‐Tønnessen Bernt Johan³⁴,Vigeland Magnus Dehli¹²,Amundsen Silja Svanstrøm²,Ribarska Teodora¹²,Åsten Pamela Marika⁵,Sheng Ying²,Helseth Eirik¹⁴,Gilfillan Gregor Duncan¹²,Mero Inger‐Lise²,Heimdal Ketil Riddervold²³

Affiliation:

1. Faculty of Medicine University of Oslo Oslo Norway

2. Department of Medical Genetics Oslo University Hospital Oslo Norway

3. Norwegian National Unit for Craniofacial Surgery Oslo University Hospital Oslo Norway

4. Department of Neurosurgery Oslo University Hospital Oslo Norway

5. TAKO Centre, Lovisenberg Diakonale Hospital Oslo Norway

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62663