D. Williams

Large-scale discovery of novel genetic causes of developmental disorders

Tomas W. Fitzgerald, M. Hurles, J. Barrett, 2014, Nature.

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

G. J. Swaminathan, N. Carter, M. Hurles, 2019, American journal of human genetics.

Evolving fetal phenotypes and clinical impact of progressive prenatal exome sequencing pathways: cohort study

M. Kilby, D. McMullan, D. Williams, 2021, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta‐analysis

D. McMullan, D. Williams, S. Hillman, 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies

M. Kilby, L. Chitty, E. Maher, 2021, BJOG : an international journal of obstetrics and gynaecology.

Microarray comparative genomic hybridization in prenatal diagnosis: a review

D. McMullan, D. Williams, S. Hillman, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta‐analysis

M. Kilby, A. Coomarasamy, D. McMullan, 2014, BJOG : an international journal of obstetrics and gynaecology.