BRCA1 and BRCA2 mutation spectrum – an update on mutation distribution in a large cancer genetics clinic in Norway

por Heramb, Cecilie, Wangensteen, Teresia, Grindedal, Eli Marie, Ariansen, Sarah Louise, Lothe, Sheba, Heimdal, Ketil Riddervold, Mæhle, Lovise
Publicado 2018

Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis

por Tønne, Elin, Due-Tønnessen, Bernt Johan, Mero, Inger-Lise, Wiig, Ulrikke Straume, Kulseth, Mari Ann, Vigeland, Magnus Dehli, Sheng, Ying, von der Lippe, Charlotte, Tveten, Kristian, Meling, Torstein Ragnar, Helseth, Eirik, Heimdal, Ketil Riddervold
Publicado 2020