Normal activity and electrophoretic mobility of erythrocyte glucose-6-phosphate dehydrogenase in males with X-linked mental retardation and the fragile Xq.

Por Carroll, A J, Howard-Peebles, P N
Publicado em 1981

Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.

Por Hittner, H M, Carroll, A J, Prchal, J T
Publicado em 1982

An unbalanced (6q;13q) translocation in a male with clinical features of Ehlers-Danlos type II syndrome.

Por Scarbrough, P R, Daw, J, Carroll, A J, Finley, S C
Publicado em 1984

Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocation.

Por Scarbrough, P R, Carroll, A J, Finley, S C, Hamerick, K
Publicado em 1986

Light-chain gene expression before heavy-chain gene rearrangement in pre-B cells transformed by Epstein-Barr virus.

Por Kubagawa, H, Cooper, M D, Carroll, A J, Burrows, P D
Publicado em 1989

Paternal Robertsonian translocation t(13q;14q) and maternal reciprocal translocation t(7p;13q) in a couple with repeated fetal loss.

Por Scarbrough, P R, Carroll, A J, Younger, J B, Finley, S C
Publicado em 1984

A de novo 3p;8p unbalanced translocation resulting in partial dup(3p) and partial del(8p).

Por Scarbrough, P R, Carroll, A J, Finley, W H, Bridges, D R
Publicado em 1987

Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.

Por Keppler-Noreuil, K M, Carroll, A J, Finley, W H, Rutledge, S L
Publicado em 1995

Identification of a recombination event narrowing the Lafora disease gene region.

Por Maddox, L O, Descartes, M, Collins, J, Keating, J, Rosenfeld, S, Palmer, C, Carroll, A J, Kuzniecky, R
Publicado em 1997

Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.

Por Münke, M, Foellmer, B, Watkins, P C, Cowan, J M, Carroll, A J, Gusella, J F, Francke, U
Publicado em 1988

The t(10;14)(q24;q11) of T-cell acute lymphoblastic leukemia juxtaposes the delta T-cell receptor with TCL3, a conserved and activated locus at 10q24.

Por Zutter, M, Hockett, R D, Roberts, C W, McGuire, E A, Bloomstone, J, Morton, C C, Deaven, L L, Crist, W M, Carroll, A J, Korsmeyer, S J
Publicado em 1990

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia

Por Eisfeld, A-K, Mrózek, K, Kohlschmidt, J, Nicolet, D, Orwick, S, Walker, C J, Kroll, K W, Blachly, J S, Carroll, A J, Kolitz, J E, Powell, B L, Wang, E S, Stone, R M, de la Chapelle, A, Byrd, J C, Bloomfield, C D
Publicado no Leukemia (2017)

Targetable Kinase-Activating Lesions in Ph-like Acute Lymphoblastic Leukemia

Por Roberts, K.G., Li, Y., Payne-Turner, D., Harvey, R.C., Yang, Y.-L., Pei, D., McCastlain, K., Ding, L., Lu, C., Song, G., Ma, J., Becksfort, J., Rusch, M., Chen, S.-C., Easton, J., Cheng, J., Boggs, K., Santiago-Morales, N., Iacobucci, I., Fulton, R.S., Wen, J., Valentine, M., Cheng, C., Paugh, S.W., Devidas, M., Chen, I-M., Reshmi, S., Smith, A., Hedlund, E., Gupta, P., Nagahawatte, P., Wu, G., Chen, X., Yergeau, D., Vadodaria, B., Mulder, H., Winick, N.J., Larsen, E.C., Carroll, W.L., Heerema, N.A., Carroll, A.J., Grayson, G., Tasian, S.K., Moore, A.S., Keller, F., Frei-Jones, M., Whitlock, J.A., Raetz, E.A., White, D.L., Hughes, T.P., Auvil, J.M. Guidry, Smith, M.A., Marcucci, G., Bloomfield, C.D., Mrózek, K., Kohlschmidt, J., Stock, W., Kornblau, S.M., Konopleva, M., Paietta, E., Pui, C.-H., Jeha, S., Relling, M.V., Evans, W.E., Gerhard, D.S., Gastier-Foster, J.M., Mardis, E., Wilson, R.K., Loh, M.L., Downing, J.R., Hunger, S.P., Willman, C.L., Zhang, J., Mullighan, C.G.
Publicado em 2014