Marianne Schwartz

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.

Genetic heterogeneity among blue-cone monochromats.

J. Nathans, L. Sharpe, E. Zrenner, 1993, American journal of human genetics.

A novel arginine‐to‐cysteine substitution in the triple helical region of the α1(I) collagen chain in a family with an osteogenesis imperfecta/Ehlers–Danlos phenotype

M. Schwartz, M. Duno, E. Christensen, 2007, Clinical genetics.

Screening for Carriers of Cystic Fibrosis among Pregnant Women: A Pilot Study

M. Schwartz, F. Skovby, N. Brandt, 1993, European journal of human genetics : EJHG.