Fiona S. Togneri
Edgbaston, ENG B152TG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Cytogenomic results following high-chance non-invasive prenatal testing: a UK national audit.
Journal: Genetics research
Published: September 02, 2020
Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics Laboratory.
Journal: Genetics research
Published: December 10, 2019
Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.
Journal: Prenatal diagnosis
Published: May 27, 2019
Second-trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray.
Journal: Clinical case reports
Published: September 21, 2018
Comparing mutation calls in fixed tumour samples between the affymetrix OncoScan® array and PCR based next-generation sequencing.
Journal: BMC medical genomics
Published: June 07, 2016
Germline ESR2 mutation predisposes to medullary thyroid carcinoma and causes up-regulation of RET expression.
Journal: Human molecular genetics
Published: December 31, 2015
Genomic complexity of urothelial bladder cancer revealed in urinary cfDNA.
Journal: European journal of human genetics : EJHG
Published: June 02, 2015
Cross-laboratory validation of the OncoScan® FFPE Assay, a multiplex tool for whole genome tumour profiling.
Journal: BMC medical genomics
Published: October 10, 2014
Axenfeld-Rieger syndrome: further clinical and array delineation of four unrelated patients with a 4q25 microdeletion.
Journal: American journal of medical genetics. Part A
Published: August 14, 2013
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: January 14, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026