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Paper Details

Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans.
Hum Mol Genet
9
2019
Author NameAffiliation
Maya TopfInstitute of Structural and Molecular Biology, Birkbeck College
Maria Bitner-GlindziczUCL Great Ormond Street Institute of Child Health, University College London
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