Wilson RB - Search Results

1

A novel, non-nested reverse-transcriptase polymerase chain reaction (RT-PCR) test for the detection of the t(15;17) translocation: a comparative study of RT-PCR cytogenetics, and fluorescence In situ hybridization.

Rennert H, Golde T, Wilson RB, Spitalnik SL, Van Deerlin VM, Leonard DG. Rennert H, et al. Among authors: wilson rb. Mol Diagn. 1999 Sep;4(3):195-209. doi: 10.1016/s1084-8592(99)80023-x. Mol Diagn. 1999. PMID: 10553020

2

Detection of clonal T-cell receptor gamma gene rearrangements using fluorescent-based PCR and automated high-resolution capillary electrophoresis.

Luo V, Lessin SR, Wilson RB, Rennert H, Tozer C, Benoit B, Leonard DG. Luo V, et al. Among authors: wilson rb. Mol Diagn. 2001 Sep;6(3):169-79. doi: 10.1054/modi.2001.27056. Mol Diagn. 2001. PMID: 11571710

3

Novel bcl-2 breakpoints in patients with follicular lymphoma.

Wang YL, Addya K, Edwards RH, Rennert H, Dodson L, Leonard DG, Wilson RB. Wang YL, et al. Among authors: wilson rb. Diagn Mol Pathol. 1998 Apr;7(2):85-9. doi: 10.1097/00019606-199804000-00004. Diagn Mol Pathol. 1998. PMID: 9785006

4

Spinal muscular atrophy genetic testing experience at an academic medical center.

Ogino S, Leonard DG, Rennert H, Wilson RB. Ogino S, et al. Among authors: wilson rb. J Mol Diagn. 2002 Feb;4(1):53-8. doi: 10.1016/S1525-1578(10)60680-0. J Mol Diagn. 2002. PMID: 11826188 Free PMC article.

5

Detection of leukemia-associated MLL-GAS7 translocation early during chemotherapy with DNA topoisomerase II inhibitors.

Megonigal MD, Cheung NK, Rappaport EF, Nowell PC, Wilson RB, Jones DH, Addya K, Leonard DG, Kushner BH, Williams TM, Lange BJ, Felix CA. Megonigal MD, et al. Among authors: wilson rb. Proc Natl Acad Sci U S A. 2000 Mar 14;97(6):2814-9. doi: 10.1073/pnas.050397097. Proc Natl Acad Sci U S A. 2000. PMID: 10706619 Free PMC article.

6

Heteroduplex formation in SMN gene dosage analysis.

Ogino S, Leonard DG, Rennert H, Gao S, Wilson RB. Ogino S, et al. Among authors: wilson rb. J Mol Diagn. 2001 Nov;3(4):150-7. doi: 10.1016/S1525-1578(10)60666-6. J Mol Diagn. 2001. PMID: 11687598 Free PMC article.

7

Duplications and de novo deletions of the SMNt gene demonstrated by fluorescence-based carrier testing for spinal muscular atrophy.

Chen KL, Wang YL, Rennert H, Joshi I, Mills JK, Leonard DG, Wilson RB. Chen KL, et al. Among authors: wilson rb. Am J Med Genet. 1999 Aug 27;85(5):463-9. Am J Med Genet. 1999. PMID: 10405443

8

Genetic risk assessment in carrier testing for spinal muscular atrophy.

Ogino S, Leonard DG, Rennert H, Ewens WJ, Wilson RB. Ogino S, et al. Among authors: wilson rb. Am J Med Genet. 2002 Jul 15;110(4):301-7. doi: 10.1002/ajmg.10425. Am J Med Genet. 2002. PMID: 12116201

9

Designer red cells.

Wilson RB, Spitalnik SL. Wilson RB, et al. Transfusion. 1994 Mar;34(3):189-91. doi: 10.1046/j.1537-2995.1994.34394196613.x. Transfusion. 1994. PMID: 8146889 No abstract available.

10

Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1.

Ogino S, Gao S, Leonard DG, Paessler M, Wilson RB. Ogino S, et al. Among authors: wilson rb. Eur J Hum Genet. 2003 Mar;11(3):275-7. doi: 10.1038/sj.ejhg.5200957. Eur J Hum Genet. 2003. PMID: 12673282

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