The Merit(nTOF-11) High Intensity Liquid Mercury Target Experiment at the CERN PS (2008)
Efthymiopoulos, I, Bennett, J R J, Caretta, O, Carroll, A J, Fabich, A, Graves, V B, ...
The MERIT(nTOF-11) experiment is a proof-ofprinciple test of a target system for a high power proton beam to be used as front-end for a neutrino factory or a muon collider. The experiment took data...
Moorman, A.V., Raimondi, S.C., Pui, C.H., Baruchel, A., Biondi, A., Carroll, A.J., ...
This study characterized the additional chromosomal abnormalities (ACA) associated with 11q23 rearrangements in 450 infants and children with acute lymphoblastic leukemia (ALL) and examined the...
Heerema, N.A., Harbott, J., Galimberti, S., Camitta, B.M., Gaynon, P.S., Janka-Schaub, G., ...
Additional chromosomal aberrations occur frequently in Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia (ALL) of childhood. The treatment outcome of these patients is...
Zutter, M, Hockett, R D, Roberts, C W, McGuire, E A, Bloomstone, J, Morton, C C, ...
We cloned the t(10;14) recurrent translocation from CD3-negative T-cell acute lymphoblastic leukemia cells. The breakpoint at 14q11 involved an intermediate rearrangement of the delta T-cell receptor...
Kubagawa, H, Cooper, M D, Carroll, A J, Burrows, P D
Epstein-Barr virus transformation of B-cell-depleted bone marrow cells from human fetuses allowed us to identify novel cell types characterized by the expression of immunoglobulin kappa or lambda...
Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.
Hittner, H M, Carroll, A J, Prchal, J T
A black family with two male infants affected with the X-linked Lowe syndrome was studied. All three females in the pedigree were found to be carriers on the basis of lenticular opacities. Each...
Zutter, M, Hockett, R D, Roberts, C W, McGuire, E A, Bloomstone, J, Morton, C C, ...
We cloned the t(10;14) recurrent translocation from CD3-negative T-cell acute lymphoblastic leukemia cells. The breakpoint at 14q11 involved an intermediate rearrangement of the delta T-cell receptor...
Kubagawa, H, Cooper, M D, Carroll, A J, Burrows, P D
Epstein-Barr virus transformation of B-cell-depleted bone marrow cells from human fetuses allowed us to identify novel cell types characterized by the expression of immunoglobulin kappa or lambda...
Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.
Hittner, H M, Carroll, A J, Prchal, J T
A black family with two male infants affected with the X-linked Lowe syndrome was studied. All three females in the pedigree were found to be carriers on the basis of lenticular opacities. Each...
Münke, M, Foellmer, B, Watkins, P C, Cowan, J M, Carroll, A J, Gusella, J F, ...
We have assigned six polymorphic DNA segments to chromosomal subregions and have established the physical order of these sequences on the long arm of chromosome 21 by in situ hybridization of cloned...
Scarbrough, P R, Daw, J, Carroll, A J, Finley, S C
Ehlers-Danlos syndrome has been divided into several different types according to the variety and severity of clinical manifestations, and may follow autosomal dominant, autosomal recessive, or X...
Scarbrough, P R, Carroll, A J, Younger, J B, Finley, S C
Marriages involving partners both of whom have abnormal karyotypes are rare and are usually ascertained because of a history of infertility, repeated abortions, or the birth of a balanced...
Scarbrough, P R, Carroll, A J, Finley, S C, Hamerick, K
A male infant, partially trisomic for a small segment of chromosomes 6 and 22 resulting from a maternal translocation, is described. Comparison of the phenotypic features of the proband with those...
A de novo 3p;8p unbalanced translocation resulting in partial dup(3p) and partial del(8p).
Scarbrough, P R, Carroll, A J, Finley, W H, Bridges, D R
We present the first case of a de novo translocation resulting in dup(3p). Giemsa banding studies tentatively identified the source of the extra genetic material as 3p. Clinical findings were...
Identification of a recombination event narrowing the Lafora disease gene region.
Maddox, L O, Descartes, M, Collins, J, Keating, J, Rosenfeld, S, Palmer, C, ...
Patients affected with progressive myoclonus epilepsy of the Lafora type present during late adolescence with a characteristic EEG pattern and Lafora bodies seen on skin biopsy. The critical region...
Keppler-Noreuil, K M, Carroll, A J, Finley, W H, Rutledge, S L
We report three unrelated patients with small terminal deletions involving 1p36.22-->pter that occurred de novo and compare our patients to the 10 previously reported cases. Although our patients...