Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.
Magenis Re , Litt M , Newcom , Donlon Ta
American Journal of Human Genetics 35 ( 6) 1097 -1106
32
1983
Expression of bcr-abl fusion transcripts following bone marrow transplantation for Philadelphia chromosome-positive leukemia.
Cleary Ml , Kohler S , Sklar Jl , Blume Kg
Leukemia 4 ( 8) 541 -547
35
1990
Characterization of spontaneous factor-independent cell lines derived from the human leukemic cell line TF-1: a dominant event.
Mannoni P , Lopez M , Lee F , Gabert Ja
Leukemia 8 ( 8) 1359 -1368
5
1994
Non-mosaic trisomy 16 in a third-trimester fetus.
Yancey Mk , Donlon Ta , Pacheco C , Hardin El
Obstetrics & Gynecology 87 ( 5) 856 -860
19
1996
Non-mosaic trisomy 16 in a near-term child
J.E. Murray , T.A. Donlon , C.D. Kuslich
American Journal of Human Genetics 55
1994
Deletion of locus D15S113 in a mother and son without features of Angelman syndrome
T.A. Donlon , J.C. Tarleton , R.J. Simensen , R.C. Michaelis
American Journal of Human Genetics 55
1994
Report on the genetic constitution of chromosome 16.
S.T. Reeders , T.A. Donlon
Cytogenetic and Genome Research 49 94 -94
4
1988
Localization of the human T lymphocyte activation gene 519 (D2S69E) to chromosome 2p12→q11
T.A. Donlon , A.M. Krensky , C. Clayberger
Cytogenetic and Genome Research 53 ( 4) 230 -231
9
1990
The gene for the RNA component of the mitochondrial RNA-processing endoribonuclease is located on human chromosome 9p and on mouse chromosome 4.
C.-L. Hsieh , T.A. Donlon , B.T. Darras , D.D. Chang
Genomics 6 ( 3) 540 -544
32
1990
Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12
T.A. Donlon , A.M. Krensky , M.R. Wallace , F.S. Collins
Genomics 6 ( 3) 548 -553
58
1990
Prader-Willi Syndrome Is Caused by Disruption of the SNRPN Gene
C.D. Kuslich , J.A. Kobori , G. Mohapatra , C. Gregorio-King
American Journal of Human Genetics 64 ( 1) 70 -76
60
1999
Report of the committee on the genetic constitution of chromosomes 14 and 15
D.W. Cox , T.A. Donlon
Cytogenetic and Genome Research 51 ( 1-4) 280 -298
1989
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.
T. A. Donlon , M. Lalande , A. Wyman , G. Bruns
Proceedings of the National Academy of Sciences of the United States of America 83 ( 12) 4408 -4412
131
1986
Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes.
T. A. Donlon
Human Genetics 80 ( 4) 322 -328
87
1988
FOXO3A genotype is strongly associated with human longevity
B. J. Willcox , T. A. Donlon , Q. He , R. Chen
Proceedings of the National Academy of Sciences of the United States of America 105 ( 37) 13987 -13992
693
2008
Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands
T. A. Donlon , R. E. Magenis
Human Genetics 65 ( 2) 144 -146
69
1983
Who Are the Okinawans? Ancestry, Genome Diversity, and Implications for the Genetic Study of Human Longevity From a Geographically Isolated Population
N. Bendjilali , W.-C. Hsueh , Q. He , D. C. Willcox
Journals of Gerontology Series A-biological Sciences and Medical Sciences 69 ( 12) 1474 -1484
9
2014
Genetic Analysis of TOR Complex Gene Variation With Human Longevity: A Nested Case–Control Study of American Men of Japanese Ancestry
B. J. Morris , T. A. Donlon , Q. He , J. S. Grove
Journals of Gerontology Series A-biological Sciences and Medical Sciences 70 ( 2) 133 -142
13
2015
FOXO3 Gene Variants and Human Aging: Coding Variants May Not Be Key Players
T. A. Donlon , J. D. Curb , Q. He , J. S. Grove
Journals of Gerontology Series A-biological Sciences and Medical Sciences 67 ( 11) 1132 -1139
49
2012
Association Analyses of Insulin Signaling Pathway Gene Polymorphisms With Healthy Aging and Longevity in Americans of Japanese Ancestry
B. J. Morris , T. A. Donlon , Q. He , J. S. Grove
Journals of Gerontology Series A-biological Sciences and Medical Sciences 69 ( 3) 270 -273
12
2014