Browse by Person
 | Up a level |
Number of items: 1.
Demetriou, C. and Chanudet, E. and Joseph, Agnel and Topf, Maya and Thomas, A.C. and Bitner-Glindzicz, M. and Regan, L. and Stanier, P. and Moore, G.E. (2019) Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans. Human Molecular Genetics 28 (20), pp. 3466-3474. ISSN 0964-6906.