Etiologic heterogeneity in the familial aggregation of congenital cardiovascular malformations.

Por Maestri, N E, Beaty, T H, Boughman, J A
Publicado em 1989

Multipoint mapping studies of the beta-globin, insulin, and c-Ha-ras-1 loci on 11p.

Por Meyers, D A, Beaty, T H, Maestri, N E, Antonarakis, S E, Kazazian, H H
Publicado em 1986

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Por Park, W J, Theda, C, Maestri, N E, Meyers, G A, Fryburg, J S, Dufresne, C, Cohen, M M, Jabs, E W
Publicado em 1995

Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II.

Por Kittur, S D, Hoppener, J W, Antonarakis, S E, Daniels, J D, Meyers, D A, Maestri, N E, Jansen, M, Korneluk, R G, Nelkin, B D, Kazazian, H H
Publicado em 1985