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Search Results - Finsterwalder, Katrin
Search Results - Finsterwalder, Katrin
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Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region
by
Reutlinger, Constanze
,
Helbig, Ingo
,
Gawelczyk, Barbara
,
Subero, Jose Ignacio Martin
,
Tönnies, Holger
,
Muhle, Hiltrud
,
Finsterwalder, Katrin
,
Vermeer, Sascha
,
Pfundt, Rolph
,
Sperner, Jürgen
,
Stefanova, Irina
,
Gillessen‐Kaesbach, Gabriele
,
Von Spiczak, Sarah
,
Van Baalen, Andreas
,
Boor, Rainer
,
Siebert, Reiner
,
Stephani, Ulrich
,
Caliebe, Almuth
Published in
Epilepsia (Copenhagen)
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Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach
by
von Spiczak, Sarah
,
Finsterwalder, Katrin
,
Muhle, Hiltrud
,
Franke, Andre
,
Schilhabel, Markus
,
Stephani, Ulrich
,
Helbig, Ingo
Published in
Epilepsia (Copenhagen)
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Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach: Comprehensive Analysis of PPR Candidate Genes
by
von Spiczak, Sarah
,
Finsterwalder, Katrin
,
Muhle, Hiltrud
,
Franke, Andre
,
Schilhabel, Markus
,
Stephani, Ulrich
,
Helbig, Ingo
Published in
Epilepsia (Copenhagen)
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Epilepsia
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Clinical Neurology
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Glutamate Receptor
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Humans
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Life Sciences & Biomedicine
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Neurosciences & Neurology
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Receptors, N-Methyl-D-Aspartate - Genetics
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Science & Technology
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Abnormalities, Multiple - Genetics
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Adult
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Age Of Onset
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Benign
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Bioinformatics
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Biological And Medical Sciences
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Child
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Chromosomes, Human, Pair 16 - Genetics
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Coding
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Computational Biology - Methods
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Eeg
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Electroencephalography - Statistics & Numerical Data
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Epilepsies, Partial - Genetics
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Wiley-Blackwell Journals (Backfile Content)
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