Search Results - Neuhann, Teresa M.
- Showing 1 - 2 results of 2
-
1
The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1: is it really a reversed sotos syndrome? by Dikow, Nicola (Author) , Maas, Bianca (Author) , Gaspar, Harald (Author) , Kreiss‐Nachtsheim, Martina (Author) , Engels, Hartmut (Author) , Kuechler, Alma (Author) , Garbes, Lutz (Author) , Netzer, Christian (Author) , Neuhann, Teresa M. (Author) , Koehler, Udo (Author) , Casteels, Kristina (Author) , Devriendt, Koen (Author) , Janssen, Johannes W. G. (Author) , Jauch, Anna (Author) , Hinderhofer, Katrin (Author) , Moog, Ute (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
2
Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia by Endris, Volker (Author) , Hackmann, Karl (Author) , Neuhann, Teresa M. (Author) , Grasshoff, Ute (Author) , Bonin, Michael (Author) , Haug, Ulrich (Author) , Hahn, Gabriele (Author) , Schallner, Jens C. (Author) , Schröck, Evelin (Author) , Tinschert, Sigrid (Author) , Rappold, Gudrun (Author) , Moog, Ute (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Editorial Online Resource