1-3 of 3
Adrian M Stuetz, PhD
Close
Sort by
Journal Articles

Whole Exome Sequencing Identifies Novel Lyst-Missense Mutations In Incomplete Childhood Chediak-Higashi-Syndrome Presenting As Hemphagocytic Lymphohistiocytosis (HLH)

Joachim Kunz, MD, Tobias Rausch, PhD, Obul R Bandapalli, PhD, Adrian M Stuetz, PhD, Johann Greil, MD, Ingrid Hausser, MD, Jan Korbel, PhD, Andreas E Kulozik, MD, PhD
Journal: Blood
Blood (2013) 122 (21): 3479.
https://doi.org/10.1182/blood.V122.21.3479.3479
Published: 2013
Journal Articles

Whole Exome Sequencing In Relapsed Pediatric T-ALL: Progression Into Relapse Is Characterized By An Increased Number Of Somatic Mutations and a Conservation Of Mutations In Leukemogenic Driver Genes

Joachim Kunz, MD, Tobias Rausch, PhD, Obul R Bandapalli, PhD, Martina U. Muckenthaler, PhD, Adrian M Stuetz, PhD, Martin Stanulla, MD, MSc, Martin Schrappe, MD, Rupert Handgretinger, Smadar Avigad, PhD, Jan Korbel, PhD, Andreas E. Kulozik, MD, PhD
Journal: Blood
Blood (2013) 122 (21): 228.
https://doi.org/10.1182/blood.V122.21.228.228
Published: 2013
Journal Articles

Whole-Exome Sequencing Links CARD11 Inactivation with SCID

Johann Greil, MD, Tobias Rausch, PhD, Thomas Giese, MD, Obul Reddy Bandapalli, PhD, Volker Daniel, MD, PhD, Isabelle Bekeredjian-Ding, PhD, Adrian M Stuetz, PhD, Christoph Drees, PhD, Susanne Roth, MD, Jürgen Ruland, MD, Jan Korbel, PhD, Andreas E Kulozik, MD, PhD
Journal: Blood
Blood (2012) 120 (21): 258.
https://doi.org/10.1182/blood.V120.21.258.258
Published: 2012