Joyce Fox

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.

Screening for Mycobacterium tuberculosis using an interferon-gamma release assay.

T. Simpson, Joyce Fox, K. Field, 2012, Journal of public health management and practice : JPHMP.

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

H. Dietz, A. Paepe, B. Loeys, 2006, Nature Genetics.

Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins

Justyna A. Karolak, P. Stankiewicz, P. Szafranski, 2020, The Journal of Molecular Diagnostics.

Quantitative and qualitative QuantiFERON(®)-TB gold in-tube results among groups with varying risks of exposure to tuberculosis.

T. Simpson, Joyce Fox, K. Field, 2012, Heart & lung : the journal of critical care.

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

Kristin M. Scheible, U. Surti, P. Stankiewicz, 2016, Human Genetics.

Clinical features associated with copy number variations of the 14q32 imprinted gene cluster

J. Rosenfeld, L. Shaffer, B. Ballif, 2015, American journal of medical genetics. Part A.

Highly sensitive blocker displacement amplification and droplet digital PCR reveal very low-level parental FOXF1 somatic mosaicism in families with ACDMPV.

Justyna A. Karolak, P. Stankiewicz, P. Szafranski, 2020, Journal of Molecular Diagnostics.