Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities

Adhideb Ghosh, Lucy Higgins, SA Larkins, C Miller, N Ostojic, William Martin, Mark Kilby

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)1068-1071
Number of pages4
JournalPrenatal Diagnosis
Issue number11
Publication statusPublished - 1 Nov 2008


  • fetal MRI
  • fetal imaging
  • prenatal diagnosis
  • functional Xp disomy
  • general cytogenetics prenatal cytogenetics
  • fetal ultrasound fetal imaging
  • posterior fossa abnormalities

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