A gene for dominant nonspecific X-linked mental retardation is located in Xq28.

Eitemau Tebyg

• Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.
  gan: des Portes, V, et al.
  Cyhoeddwyd: (1997)
• Refining the genetic location of the gene for X linked hydrocephalus within Xq28.
  gan: Jouet, M, et al.
  Cyhoeddwyd: (1993)
• X-Linked Mental Retardation with Seizures and Carrier Manifestations Is Caused by a Mutation in the Creatine-Transporter Gene (SLC6A8) Located in Xq28
  gan: Hahn, Kimberly A., et al.
  Cyhoeddwyd: (2002)
• A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.
  gan: Pai, G S, et al.
  Cyhoeddwyd: (1997)
• Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation
  gan: Bijlsma, E.K., et al.
  Cyhoeddwyd: (2012)