Norman–Roberts syndrome (Q130555)
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lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.
- Lissencephaly 2
- Norman-Roberts syndrome
- lissencephaly 2
- lissencephaly syndrome, Norman-Roberts type
- Microlissencephaly type A
- Lissencephaly type 2
- LISSENCEPHALY 2; LIS2
- LIS2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Norman–Roberts syndrome |
lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22. |
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Wikipedia(6 entries)
- bswiki Norman-Robertsov sindrom
- dewiki Norman-Roberts-Syndrom
- enwiki Norman–Roberts syndrome
- fiwiki Norman–Robertsin lissenkefaliaoireyhtymä
- nlwiki Type-2-lissencefalie
- ruwiki Синдром Норман — Робертс