Apolipoprotein A-I gene polymorphism and susceptibility of non-insulin-dependent diabetes mellitus.

Por Buraczynska, M, Hanzlik, J, Grzywa, M
Publicado em 1985

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Por Fujita, R, Buraczynska, M, Gieser, L, Wu, W, Forsythe, P, Abrahamson, M, Jacobson, S G, Sieving, P A, Andréasson, S, Swaroop, A
Publicado em 1997

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.

Por Buraczynska, M, Wu, W, Fujita, R, Buraczynska, K, Phelps, E, Andréasson, S, Bennett, J, Birch, D G, Fishman, G A, Hoffman, D R, Inana, G, Jacobson, S G, Musarella, M A, Sieving, P A, Swaroop, A
Publicado em 1997

Trisomy 21: Association between reduced recombination and nondisjunction

Por Sherman, S. L., Takaesu, N., Freeman, S. B., Grantham, M., Phillips, C., Blackston, R. D., Jacobs, P. A., Cockwell, A. E., Freeman, V., Uchida, I., Mikkelsen, M., Kurnit, D. M., Buraczynska, M., Keats, B. J. B., Hassold, T. J.
Publicado em 1991