@article{Ellard:2026:10.1136/jmg-2026-111522,
author = {Ellard, S and Hanson, H and Cassidy, E-J and Thomson, K and Durkie, M and Berry, I and Mann, K and Mein, R and Stals, K and Rankin, J and Taylor, RW and McVeigh, TP and Snape, K and Turnbull, C and Clancy, T and Lucassen, A and Deans, ZC and Ware, J and Baple, EL},
doi = {10.1136/jmg-2026-111522},
journal = {J Med Genet},
pages = {697--706},
title = {The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.},
url = {http://dx.doi.org/10.1136/jmg-2026-111522},
volume = {63},
year = {2026}
}

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TY  - JOUR
AU  - Ellard,S
AU  - Hanson,H
AU  - Cassidy,E-J
AU  - Thomson,K
AU  - Durkie,M
AU  - Berry,I
AU  - Mann,K
AU  - Mein,R
AU  - Stals,K
AU  - Rankin,J
AU  - Taylor,RW
AU  - McVeigh,TP
AU  - Snape,K
AU  - Turnbull,C
AU  - Clancy,T
AU  - Lucassen,A
AU  - Deans,ZC
AU  - Ware,J
AU  - Baple,EL
DO  - 10.1136/jmg-2026-111522
EP  - 706
PY  - 2026///
SP  - 697
TI  - The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.
T2  - J Med Genet
UR  - http://dx.doi.org/10.1136/jmg-2026-111522
UR  - https://www.ncbi.nlm.nih.gov/pubmed/42562627
VL  - 63
ER  - 

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