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Search Results - Munk‐Schulenburg, Susanne
Search Results - Munk‐Schulenburg, Susanne
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High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one‐third of probands are minors
by
Spiegler, Stefanie
,
Najm, Juliane
,
Liu, Jian
,
Gkalympoudis, Stephanie
,
Schröder, Winnie
,
Borck, Guntram
,
Brockmann, Knut
,
Elbracht, Miriam
,
Fauth, Christine
,
Ferbert, Andreas
,
Freudenberg, Leonie
,
Grasshoff, Ute
,
Hellenbroich, Yorck
,
Henn, Wolfram
,
Hoffjan, Sabine
,
Hüning, Irina
,
Korenke, G. Christoph
,
Kroisel, Peter M.
,
Kunstmann, Erdmute
,
Mair, Martina
,
Munk‐Schulenburg, Susanne
,
Nikoubashman, Omid
,
Pauli, Silke
,
Rudnik‐Schöneborn, Sabine
,
Sudholt, Irene
,
Sure, Ulrich
,
Tinschert, Sigrid
,
Wiednig, Michaela
,
Zoll, Barbara
,
Ginsberg, Mark H.
,
Felbor, Ute
Published in
Molecular genetics & genomic medicine
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SALL1 mutations in sporadic Townes-Brocks syndrome are of predominantly paternal origin without obvious paternal age effect
by
Böhm, Johann
,
Munk-Schulenburg, Susanne
,
Felscher, Stephanie
,
Kohlhase, Jürgen
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics. Part A
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Molecular Genetics & Genomic Medicine
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Genetics & Heredity
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Ccm1
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Ccm2 Protein
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Cerebral Cavernous Malformation
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Ethylenediaminetetraacetic Acid
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