Sinnott, P., Collier, S., Costigan, C., Dyer, P. A., Harris, R., & Strachan, T. (1990). Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

Sinnott, P., S. Collier, C. Costigan, P A. Dyer, R. Harris, and T. Strachan. Genesis By Meiotic Unequal Crossover of a De Novo Deletion That Contributes to Steroid 21-hydroxylase Deficiency. 1990.

Sinnott, P., et al. Genesis By Meiotic Unequal Crossover of a De Novo Deletion That Contributes to Steroid 21-hydroxylase Deficiency. 1990.