P096: QRICH1-related disorder: Phenotype expansion vs blended phenotype

Documenti analoghi

• P321: Expanding the phenotypic spectrum of Currarino syndrome with cardiac anomalies
  di: Vanina Taliercio, et al.
  Pubblicazione: (2023-01-01)
• P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
  di: Stacey Cole, et al.
  Pubblicazione: (2024-01-01)
• P166: MEK inhibitor therapy for lymphatic malformations: A focused approach in patients with RASopathies*
  di: Vanina Taliercio, et al.
  Pubblicazione: (2024-01-01)
• P096: Withdrawn
  Pubblicazione: (2024-01-01)
• An expansion of the phenotype in individuals with SYNCRIP-Related Neurodevelopmental Disorder
  di: Tooba Shafiq, et al.
  Pubblicazione: (2024-01-01)