B. Goodwin

Maternal age specific risk rate estimates for Down syndrome among live births in whites and other races from Ohio and metropolitan Atlanta, 1970-1989.

C. Huether, J. Ivanovich, B. Goodwin, 1998, Journal of medical genetics.

A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report

M. Jaeger, M. Netea, B. Goodwin, 2018, BMC Medical Genetics.

A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report

M. Jaeger, M. Netea, B. Goodwin, 2018, BMC Medical Genetics.

Estimation of prevalence of transthyretin (ATTR) cardiac amyloidosis in an Australian subpopulation using bone scans with echocardiography and clinical correlation

B. Goodwin, S. Ramsay, S. Prasad, 2020, Journal of Nuclear Cardiology.

New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.

E. Haan, B. Goodwin, T. Cox, 2000, Human molecular genetics.

Autonomous thyroid nodule: Not just a disease of adulthood

B. Goodwin, Emily J Perry, L. Conwell, 2019, Journal of paediatrics and child health.