Elizabeth Quinlan-Jones
3PUBLICATIONS
6CO-AUTHORS
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Publications (3)
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|Mar 19, 2020
Second-trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray.Malgorzata Drozniewska, Mark D Kilby, Julie Vogt
|Jan 30, 2018
The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder.Victoria Hodgetts Morton, Elizabeth Quinlan-Jones, Natasha Butts
|Oct 20, 2017
Parental experiences of prenatal whole exome sequencing (WES) in cases of ultrasound diagnosed fetal structural anomaly.Elizabeth Quinlan-Jones, Sarah C Hillman, Mark D Kilby
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