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- Morris-Rosendahl, Deborah J
- Kakar, Naseebullah 2
- Kubisch, Christian 2
- Nürnberg, Peter 2
- Ahmad, Jamil 1
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STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly
- Kakar, Naseebullah
- Ahmad, Jamil
- Morris-Rosendahl, Deborah J
- Altmüller, Janine
- Friedrich, Katrin
- Barbi, Gotthold
- Nürnberg, Peter
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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
- Kortüm, Fanny
- Das, Soma
- Flindt, Max
- Morris-Rosendahl, Deborah J
- Stefanova, Irina
- Goldstein, Amy
- Horn, Denise
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New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish.
- Morris-Rosendahl, Deborah J
- Segel, Reeval
- Born, A Peter
- Conrad, Christoph
- Loeys, Bart
- Brooks, Susan Sklower
- Müller, Laura