Reply to Burghes.

Por MacKenzie, A E
Publicado em 1998

The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.

Por Shutler, G. G., MacKenzie, A. E., Korneluk, R. G.
Publicado em 1994

An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3

Por Shutler, G., Leblond, S., Bailly, J., MacKenzie, A.E., Tsilfidis, C., Korneluk, R.G.
Publicado em 1991

Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.

Por MacKenzie, A E, MacLeod, H L, Hunter, A G, Korneluk, R G
Publicado em 1989

GPR35 as a Novel Therapeutic Target

Por MacKenzie, A. E., Lappin, J. E., Taylor, D. L., Nicklin, S. A., Milligan, G.
Publicado em 2011

A Bsu36I RFLP detected by the chromosome 19q probe p alpha.5B [D19S36]

Por Korneluk, R G, MacLeod, H L, Leblond, S, McKeithan, T W, MacKenzie, A E
Publicado em 1989

A BanI polymorphism identified by the probe p alpha 1.4P at 19q13.1 [D19S37]

Por Korneluk, R G, MacLeod, H L, Lahey, D, McKeithan, T W, MacKenzie, A E
Publicado em 1989

Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophy.

Por Barceló, J. M., Pluscauskas, M., MacKenzie, A. E., Tsilfidis, C., Narang, M., Korneluk, R. G.
Publicado em 1994

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

Por Tsilfidis, C, MacKenzie, A E, Shutler, G, Leblond, S, Bailly, J, Johnson, K, Williamson, R, Siegel-Bartelt, J, Korneluk, R G, Shelbourne, P
Publicado em 1991