Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C

Ähnliche Einträge

• Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant
  von: Carly M. Smith, et al.
  Veröffentlicht: (2024)
• Prenatal diagnosis of ROR‐2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities
  von: Liying Yang, et al.
  Veröffentlicht: (2024)
• Shortened and Hypomineralized Bones, Renal Agenesis, and a Heart Defect: Prenatal Diagnosis of a GLI3 Variant
  von: Alexandra M. Dinu, et al.
  Veröffentlicht: (2025)
• Hereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care
  von: Carly M. Smith, et al.
  Veröffentlicht: (2026)
• Prenatal detection rates for congenital heart disease using abnormal obstetrical screening ultrasound alone as indication for fetal echocardiography
  von: Sanjay Vepa, et al.
  Veröffentlicht: (2024)