P331: WGS/WES as unique diagnostic tool for the genetic screening of patients with craniosynostosis
Alexandra Topa,
Anna Rohlin,
André Fehr,
Lovisa Lovmar,
Göran Stenman,
Peter Tarnow,
Giovanni Maltese,
Madiha Bhatti-Søfteland,
Lars Kölby
Affiliations
Alexandra Topa
1Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden; Department of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden
Anna Rohlin
Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden
André Fehr
Department of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden; Department of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden
Lovisa Lovmar
Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden
Göran Stenman
Department of Laboratory Medicine, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden; Department of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden
Peter Tarnow
Department of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden
Giovanni Maltese
Department of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden
Madiha Bhatti-Søfteland
Department of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden
Lars Kölby
Department of Plastic Surgery, University of Gothenburg, Sahlgrenska Academy, Gothenburg, Sweden
