J. Horwitz

Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency.

A. Donnenfeld, D. Cutillo, J. Knops, 2006, American journal of obstetrics and gynecology.

First report of prenatal biochemical diagnosis of Lowe syndrome

R. Nussbaum, W. O'Brien, S. Suchy, 1998, Prenatal diagnosis.

The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements

L. Shaffer, C. McCaskill, V. Reid Sutton, 2002, Prenatal diagnosis.

Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes.

L. Shaffer, S. A. Berend, C. McCaskill, 2000, American journal of human genetics.

Molecular genetic testing of a fetus at risk of Gerstmann-Sträussler-Scheinker syndrome

P. Brown, D. Gajdusek, L. Goldfarb, 1994, The Lancet.