Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities

Clin Res Hepatol Gastroenterol. 2021 Sep;45(5):101562. doi: 10.1016/j.clinre.2020.10.007. Epub 2020 Nov 15.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Congenital Abnormalities* / diagnosis
  • Congenital Abnormalities* / genetics
  • Female
  • Forkhead Transcription Factors* / genetics
  • Humans
  • Pregnancy
  • Prenatal Diagnosis

Substances

  • FOXF1 protein, human
  • Forkhead Transcription Factors