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1 Ergebnisse
1
Whole‐exome sequencing in syndromic craniosynostosis increa..:
Tønne, Elin
;
Due‐Tønnessen, Bernt Johan
;
Vigeland, Magnus Dehli
...
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1464-1475 , 2022
Link:
https://doi.org/10.1002/ajmg.a.62663
RT Journal T1
Whole‐exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.62663&Exemplar=1&LAN=DE A1 Tønne, Elin A1 Due‐Tønnessen, Bernt Johan A1 Vigeland, Magnus Dehli A1 Amundsen, Silja Svanstrøm A1 Ribarska, Teodora A1 Åsten, Pamela Marika A1 Sheng, Ying A1 Helseth, Eirik A1 Gilfillan, Gregor Duncan A1 Mero, Inger‐Lise A1 Heimdal, Ketil Riddervold PB Wiley YR 2022 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 188 IS 5 SP 1464 OP 1475 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.62663 DO https://doi.org/10.1002/ajmg.a.62663 SF ELIB - SuUB Bremen
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