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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 |
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| Authors: | A. Ghosh L. Higgins S. A. Larkins C. Miller N. Ostojic W. L. Martin M. D. Kilby |
| Affiliation: | 1. Department of Fetal Medicine, Division of Reproductive and Child Health, Birmingham Women's Hospital, University of Birmingham, Edgbaston, Birmingham, UK;2. Regional Genetics Laboratory, Birmingham Women's Hospital, Edgbaston, Birmingham UK;3. Department of Radiology, Birmingham Children's Hospital, Birmingham, UK;4. Department of Pathology, Birmingham Women's Hospital, Edgbaston, Birmingham UK |
| Abstract: | |
| Keywords: | prenatal diagnosis posterior fossa abnormalities functional Xp disomy fetal ultrasound fetal imaging fetal MRI fetal imaging general cytogenetics prenatal cytogenetics |