S. Connors

A pilot study of exome sequencing in a diverse New Zealand cohort with undiagnosed disorders and cancer

S. Robertson, C. Print, C. Blenkiron, 2018 .

An activating variant in CTNNB1 is associated with a sclerosing bone dysplasia and adrenocortical neoplasia.

S. Robertson, A. Zankl, D. Markie, 2020, The Journal of clinical endocrinology and metabolism.

Preferential expression of variable region heavy chain gene segments by predominant 2,4-dinitrophenyl-specific BALB/c neonatal antibody clonotypes.

R. Ogata, N. Klinman, S. Connors, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Transient response to imatinib mesylate (STI571) in a patient with the ETV6-ABL t(9;12) translocation.

J. Melo, S. O’Brien, R. Capdeville, 2002, Blood.

Association of Clinical Cytogeneticists chorion villus sampling database 1987–2000

S. Connors, J. Wolstenholme, J. Emslie, 2006, Prenatal diagnosis.

A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

Janice S. Lee, M. Leppert, F. Collins, 2017, Nature Communications.