Prenatal Diagnosis of Ververi‐Brady Syndrome Associated With a Novel Nonsense QRICH1 Variant: A Case Presentation

Documenti analoghi

• Prenatal Diagnosis of Arboleda‐Tham Syndrome Associated With KAT6A Variants Presented With Interrupted Inferior Vena Cava and Fetal Growth Restriction
  di: Qiu‐Xia Yu, et al.
  Pubblicazione: (2025)
• Prenatal Diagnosis of Verheij Syndrome Associated With PUF60 Variants Presented With Ventricular Septal Defect and Scoliosis Identified by First Trimester Ultrasound
  di: Ru Li, et al.
  Pubblicazione: (2025)
• Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder
  di: Xiang‐Yi Jing, et al.
  Pubblicazione: (2025)
• Prenatal Diagnosis of MED11‐Related Condition in a Family Presented With Recurrent Increased Nuchal Translucency and Hydrops Fetalis
  di: Li Zhen, et al.
  Pubblicazione: (2025)
• Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome
  di: Mia B. Hodges, et al.
  Pubblicazione: (2025)