TY  - JOUR

T1  - A cryptic CBFB deletion–inversion expands the mutational spectrum of variants associated with cleidocranial dysplasia

JO  - Clinical Genetics

UR  - https://eprints.whiterose.ac.uk/id/eprint/223087

PY  - 2025/02/02

AU  - Pagnamenta AT

AU  - Hashim M

AU  - Kennedy J

AU  - Lawton B

AU  - Offiah AC

AU  - Taylor JC

AU  - Smithson SF

ED  - 

DO  - DOI: 10.1111/cge.14709

PB  - Wiley

VL  - 108

IS  - 1

SP  - 86

EP  - 91

Y2  - 2025/11/11

ER  -