S. Olson

Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T

C. Strom, F. Hantash, J. Redman, 2004, Genetics in Medicine.

Unilateral microfibrillar abnormalities in a case of asymmetric Marfan syndrome.

M. Valli, G. Cetta, D. Hollister, 1990, American journal of human genetics.

A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia.

Y. Akkari, Fei Yang, G. Fan, 2022, Cancer genetics.

The need to reevaluate trisomy screening for advanced maternal age in prenatal diagnosis.

K. Kennedy, B. Clark, S. Olson, 1993, American journal of obstetrics and gynecology.

Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish population.

Weimin Sun, C. Strom, F. Hantash, 2006, The Journal of molecular diagnostics : JMD.

Characterization of a Recently-Discovered Mutant Fetal Hemoglobin

A. Sarkar, S. Olson, 2009 .