Norman–Roberts syndrome (Q130555)

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A 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
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English
Norman–Roberts syndrome
A 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

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