A. Vianna-Morgante

Deletion of the centromere as a mechanism for achieving stability of a dicentric chromosome.

C. Rosenberg, A. Vianna-Morgante, A. Vianna‐Morgante, 1986, Cytogenetics and cell genetics.

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

L. Vissers, B. D. de Vries, E. Eichler, 2008, Journal of Medical Genetics.

PLP1 duplication at the breakpoint regions of an apparently balanced t(X;22) translocation causes Pelizaeus–Merzbacher disease in a girl

F. Kok, A. Bonaldi, A. Vianna-Morgante, 2013, Clinical genetics.

Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome

H. van Bokhoven, C. Rosenberg, K. Szuhai, 2010, Clinical genetics.

Identification of a supernumerary marker derived from chromosome 17 using FISH.

C. Rosenberg, L. Sichero, C. Borovik, 1995, American journal of medical genetics.

Deletion of the short arm of chromosome 20

A. Richieri‐Costa, C. Rosenberg, A. Vianna-Morgante, 1987, Clinical genetics.

Selection of adrenal tumor cells in culture demonstrated by interphase cytogenetics.

A. Latronico, C. Rosenberg, B. Mendonca, 1995, Cancer genetics and cytogenetics.

Intragenic reorganization of RB1 in a complex (4;13) rearrangement demonstrated by FISH.

A. Børresen, C. Rosenberg, A. Vianna-Morgante, 1994, Cytogenetics and cell genetics.