Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.

Por Brzustowicz, L M, Wang, C H, Matseoane, D, Kleyn, P W, Vitale, E, Das, K, Penchaszadeh, G K, Munsat, T L, Hausmanowa-Petrusewicz, I, Gilliam, T C
Publicado em 1995

Paternal Isodisomy for Chromosome 5 in a Child with Spinal Muscular Atrophy

Por Brzustowicz, L. M., Allitto, B. A., Matseoane, D., Theve, R., Michaud, L., Chatkupt, S., Sugarman, E., Penchaszadeh, G. K., Suslak, L., Koenigsberger, M. R., Gilliam, T. C., Handelin, B. L.
Publicado em 1994

No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees.

Por Knowles, J A, Rao, P A, Cox-Matise, T, Loth, J E, de Jesus, G M, Levine, L, Das, K, Penchaszadeh, G K, Alexander, J R, Lerer, B, Endicott, J, Ott, J, Gilliam, T C, Baron, M
Publicado em 1998

Refinement of the Spinal Muscular Atrophy Locus by Genetic and Physical Mapping

Por Wang, C. H., Kleyn, P. W., Vitale, E., Ross, B. M., Lien, L., Xu, J., Carter, T. A., Brzustowicz, L. M., Obici, S., Selig, S., Pavone, L., Parano, E., Penchaszadeh, G. K., Munsat, T., Kunkel, L. M., Gilliam, T. C.
Publicado em 1995

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

Por Shah, A B, Chernov, I, Zhang, H T, Ross, B M, Das, K, Lutsenko, S, Parano, E, Pavone, L, Evgrafov, O, Ivanova-Smolenskaya, I A, Annerén, G, Westermark, K, Urrutia, F H, Penchaszadeh, G K, Sternlieb, I, Scheinberg, I H, Gilliam, T C, Petrukhin, K
Publicado em 1997