Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product

Similar Items

• Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product
  od: Honghong Zhang, i dr.
  Izdano: (2021-10-01)
• MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome
  od: Ryo Takeguchi, i dr.
  Izdano: (2020-02-01)
• Updating the profile of C-terminal MECP2 deletions in Rett syndrome
  od: Bebbington, A, i dr.
  Izdano: (2009)
• Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome
  od: Liraz Keidar, i dr.
  Izdano: (2019-08-01)
• Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis
  od: Vidal, Silvia, i dr.
  Izdano: (2019)