D. McMullan

发表

Large-scale discovery of novel genetic causes of developmental disorders

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

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.

Acquired Isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations

S. Akiki, D. McMullan, M. Griffiths, 2005, Leukemia.

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.

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

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

M. Drayson, T. Stankovic, D. McMullan, 2002, Leukemia.

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.

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta‐analysis

M. Kilby, A. Coomarasamy, E. Maher, 2011, 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.

The clinical utility of genetic testing of tissues from pregnancy losses

I. Simonic, P. Batstone, L. Cresswell, 2018, BJOG : an international journal of obstetrics and gynaecology.

Prenatal exome sequencing for fetuses with structural abnormalities: the next step

M. Hurles, M. Kilby, K. Carss, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

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.

Cytogenetically cryptic AML1–ETO and CBFβ–MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia

J. Reilly, G. Wilson, A. Watmore, 2000, British journal of haematology.

Ewing's sarcoma of bone: the detection of specific transcripts in a large, consecutive series of formalin‐fixed, decalcified, paraffin‐embedded tissue samples using the reverse transcriptase‐polymerase chain reaction

J. Mcclure, R. Grimer, D. McMullan, 2006, Histopathology.

Additional information from array comparative genomic hybridisation technology over conventional karyotyping in prenatal diagnosis–a systematic review and meta-analysis

M. Kilby, A. Coomarasamy, E. Maher, 2010, Archives of Disease in Childhood: Fetal and Neonatal Edition.

Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders

R. Holt, D. Gerrelli, D. Bax, 2016, Human Genetics.

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies

E. Maher, D. McMullan, S. Hillman, 2012, BJOG : an international journal of obstetrics and gynaecology.