L. Celle

Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromere.

E. Zackai, N. Spinner, C. Shields, 2001, American journal of medical genetics.

Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypes.

I. Krantz, R. Savani, M. Mennuti, 2000, American journal of medical genetics.

TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome.

E. Zackai, K. Gripp, L. Whitaker, 1999, American journal of medical genetics.

Down syndrome congenital heart disease: A narrowed region and a candidate gene

E. Zackai, N. Spinner, G. Lyons, 2001, Genetics in Medicine.

Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.

E. Zackai, T. Shaikh, B. Emanuel, 1999, American journal of human genetics.

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

E. Zackai, T. Shaikh, B. Emanuel, 2000, American journal of human genetics.