S. Cahn

Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.

S. Baruchel, H. Witkowska, E. Vichinsky, 1991, The New England journal of medicine.

Spinocerebellar Ataxia Patient Perceptions Regarding Reproductive Options

G. Wilmot, S. Cahn, A. Rosen, 2020, Movement disorders clinical practice.