J. Taylor

发表

European Reference Network for rare adult solid cancers, statement and integration to health care systems of member states: a position paper of the ERN EURACAN

A. Idbaih, P. Casali, A. Trama, 2021, ESMO open.

Population-based analysis of POT1 variants in a cutaneous melanoma case–control cohort

D. Bishop, M. Iles, D. Adams, 2022, Journal of Medical Genetics.

Late survival after elective repair of aortic aneurysms detected by screening.

E. Shaw, J. Earnshaw, K. Poskitt, 2004, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.

A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease.

J. Connell, J. Franklyn, S. Gough, 2006, The Journal of clinical endocrinology and metabolism.

A de novo frameshift in HNRNPK causing a Kabuki‐like syndrome with nodular heterotopia

A. Pagnamenta, S. Knight, H. Stewart, 2016, Clinical genetics.

Comprehensive genetic and functional analysis of FcÎ³Rs in rituximab therapy for autoimmunity reveals a key role for FcÎ³RIIIa on NK cells

J. Barrett, A. Barton, I. Bruce, 2021, medRxiv.

Prenatal diagnosis of familial ring 21 chromosome

J. Taylor, A. Melnyk, I. Ahmed, 1995, Prenatal diagnosis.