TY  - JOUR

T1  - SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

JO  - Genetics in Medicine

UR  - https://eprints.whiterose.ac.uk/190170/

PY  - 2022/03/24

AU  - Al-Jawahiri R

AU  - Foroutan A

AU  - Kerkhof J

AU  - McConkey H

AU  - Levy M

AU  - Haghshenas S

AU  - Rooney K

AU  - Turner J

AU  - Shears D

AU  - Holder M

AU  - Lefroy H et al

ED  - 

DO  - DOI: 10.1016/j.gim.2022.02.013

PB  - Elsevier BV

VL  - 24

IS  - 6

SP  - 1261

EP  - 1273

Y2  - 2024/10/23

ER  -