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Results:
1-18
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Results: 18
Authors:
Mrozek, K
Prior, TW
Edwards, C
Marcucci, G
Carroll, AJ
Snyder, PJ
Koduru, PRK
Theil, KS
Pettenati, MJ
Archer, KJ
Caligiuri, MA
Vardiman, JW
Kolitz, JE
Larson, RA
Bloomfield, CD
Citation: K. Mrozek et al., Comparison of cytogenetic and molecular genetic detection of t(8;21) and inv(16) in a prospective series of adults with de novo acute myeloid leukemia: A cancer and leukemia group B study, J CL ONCOL, 19(9), 2001, pp. 2482-2492
Authors:
Smith, WM
Zhou, XP
Kurose, K
Gao, X
Latif, F
Kroll, T
Sugano, K
Cannistra, SA
Clinton, SK
Maher, ER
Prior, TW
Eng, C
Citation: Wm. Smith et al., Opposite association of two PPARG variants with cancer: overrepresentationof H449H in endometrial carcinoma cases and underrepresentation of P12A inrenal cell carcinoma cases, HUM GENET, 109(2), 2001, pp. 146-151
Authors:
Mailman, MD
Hemingway, T
Darsey, RL
Glasure, CE
Huang, Y
Chadwick, RB
Heinz, JW
Papp, AC
Snyder, PJ
Sedra, MS
Schafer, RW
Abuelo, DN
Reich, EW
Theil, KS
Burghes, AHM
de la Chapelle, A
Prior, TW
Citation: Md. Mailman et al., Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome, HUM GENET, 108(2), 2001, pp. 109-115
Authors:
Morrison, CD
Papp, AC
Hejmanowski, AQ
Addis, VM
Prior, TW
Citation: Cd. Morrison et al., Increased D allele frequency of the angiotensin-converting enzyme gene in pulmonary fibrosis, HUMAN PATH, 32(5), 2001, pp. 521-528
Authors:
Mendell, JR
Buzin, CH
Feng, J
Yan, J
Serrano, C
Sangani, DS
Wall, C
Prior, TW
Sommer, SS
Citation: Jr. Mendell et al., Diagnosis of Duchenne dystrophy by enhanced detection of small mutations, NEUROLOGY, 57(4), 2001, pp. 645-650
Authors:
Miller, RG
Moore, DH
Dronsky, V
Bradley, W
Barohn, R
Bryan, W
Prior, TW
Gelinas, DF
Iannaccone, S
Kissel, J
Leshner, R
Mendell, J
Mendoza, M
Russmann, B
Samaha, F
Smith, S
Citation: Rg. Miller et al., A placebo-controlled trial of gabapentin in spinal muscular atrophy, J NEUR SCI, 191(1-2), 2001, pp. 127-131
Authors:
Chadwick, RB
Pyatt, RE
Niemann, TH
Richards, SK
Johnson, CK
Stevens, MW
Meek, JE
Hampel, H
Prior, TW
de la Chapelle, A
Citation: Rb. Chadwick et al., Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma, J MED GENET, 38(7), 2001, pp. 461-466
Authors:
Gorman, TE
Julius, CJ
Barth, RF
Ng, A
Kennedy, MS
Prior, TW
Allen, J
Lasky, LC
Citation: Te. Gorman et al., Transfusion-associated graft-vs-host disease - A fatal case caused by blood from an unrelated HLA homozygous donor, AM J CLIN P, 113(5), 2000, pp. 732-737
Authors:
Monani, UR
Sendtner, M
Coovert, DD
Parsons, DW
Andreassi, C
Le, TT
Jablonka, S
Schrank, B
Rossol, W
Prior, TW
Morris, GE
Burghes, AHM
Citation: Ur. Monani et al., The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy, HUM MOL GEN, 9(3), 2000, pp. 333-339
Authors:
Baschinsky, DY
Isa, A
Niemann, TH
Prior, TW
Lucas, JG
Frankel, WL
Citation: Dy. Baschinsky et al., Diffuse leiomyomatosis of the uterus: A case report with clonality analysis, HUMAN PATH, 31(11), 2000, pp. 1429-1432
Authors:
Zhou, XP
Smith, WM
Gimm, O
Mueller, E
Gao, X
Sarraf, P
Prior, TW
Plass, C
von Deimling, A
Black, PM
Yates, AJ
Eng, C
Citation: Xp. Zhou et al., Over-representation of PPAR gamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population, J MED GENET, 37(6), 2000, pp. 410-414
Authors:
Gorman, TE
Arcot, AN
Baker, P
Prior, TW
Brandt, JT
Citation: Te. Gorman et al., Prevalence of the factor V-Leiden mutation among autopsy patients with pulmonary thromboembolic disease using an improved method for factor V-Leiden detection, AM J CLIN P, 111(3), 1999, pp. 413-417
Authors:
Monani, UR
Lorson, CL
Parsons, DW
Prior, TW
Androphy, EJ
Burghes, AHM
McPherson, JD
Citation: Ur. Monani et al., A single nucleotide difference that alters splicing patterns distinguishesthe SMA gene SMN1 from the copy gene SMN2, HUM MOL GEN, 8(7), 1999, pp. 1177-1183
Authors:
Kelly, TE
Amoroso, K
Ferre, M
Blanco, J
Allinson, P
Prior, TW
Citation: Te. Kelly et al., Spinal muscular atrophy variant with congenital fractures, AM J MED G, 87(1), 1999, pp. 65-68
Authors:
Prior, TW
Chadwick, RB
Papp, AC
Arcot, AN
Isa, AM
Pearl, DK
Stemmermann, G
Percesepe, A
Loukola, A
Aaltonen, LA
de la Chapelle, A
Citation: Tw. Prior et al., The I1307K polymorphism of the APC gene in colorectal cancer, GASTROENTY, 116(1), 1999, pp. 58-63
Authors:
Mailman, MD
Muscarella, P
Schirmer, WJ
Ellison, EC
O'Dorisio, TM
Prior, TW
Citation: Md. Mailman et al., Identification of MEN1 mutations in sporadic enteropancreatic neuroendocrine tumors by analysis of paraffin-embedded tissue, CLIN CHEM, 45(1), 1999, pp. 29-34
Authors:
Pyatt, R
Chadwick, RB
Johnson, CK
Adebamowo, C
de la Chapelle, A
Prior, TW
Citation: R. Pyatt et al., Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin - Implications for microsatellite instability testing, AM J PATH, 155(2), 1999, pp. 349-353
Authors:
Parsons, DW
McAndrew, PE
Iannaccone, ST
Mendell, JR
Burghes, AHM
Prior, TW
Citation: Dw. Parsons et al., Intragenic telSMN mutations: Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number, AM J HU GEN, 63(6), 1998, pp. 1712-1723
Risultati:
1-18
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