Leonard DG - Search Results

1

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: leonard dg. 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.

2

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: leonard dg. Am J Med Genet. 2002 Jul 15;110(4):301-7. doi: 10.1002/ajmg.10425. Am J Med Genet. 2002. PMID: 12116201

3

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: leonard dg. Eur J Hum Genet. 2003 Mar;11(3):275-7. doi: 10.1038/sj.ejhg.5200957. Eur J Hum Genet. 2003. PMID: 12673282

4

Multiplex RT-PCR for the detection of leukemia-associated translocations: validation and application to routine molecular diagnostic practice.

Salto-Tellez M, Shelat SG, Benoit B, Rennert H, Carroll M, Leonard DG, Nowell P, Bagg A. Salto-Tellez M, et al. Among authors: leonard dg. J Mol Diagn. 2003 Nov;5(4):231-6. doi: 10.1016/S1525-1578(10)60479-5. J Mol Diagn. 2003. PMID: 14573782 Free PMC article.

5

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: leonard dg. Am J Med Genet. 1999 Aug 27;85(5):463-9. Am J Med Genet. 1999. PMID: 10405443

6

Heteroduplex formation in SMN gene dosage analysis.

Ogino S, Leonard DG, Rennert H, Gao S, Wilson RB. Ogino S, et al. Among authors: leonard dg. 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

SMN1 dosage analysis in spinal muscular atrophy from India.

Kesari A, Rennert H, Leonard DG, Mittal B. Kesari A, et al. Among authors: leonard dg. BMC Med Genet. 2005 May 23;6:22. doi: 10.1186/1471-2350-6-22. BMC Med Genet. 2005. PMID: 15910686 Free PMC article.

8

Prenatal diagnosis of spinal muscular atrophy: Indian scenario.

Kesari A, Rennert H, Leonard DG, Phadke SR, Mittal B. Kesari A, et al. Among authors: leonard dg. Prenat Diagn. 2005 Aug;25(8):641-4. doi: 10.1002/pd.1212. Prenat Diagn. 2005. PMID: 16049987

9

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: leonard dg. Mol Diagn. 1999 Sep;4(3):195-209. doi: 10.1016/s1084-8592(99)80023-x. Mol Diagn. 1999. PMID: 10553020

10

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: leonard dg. Mol Diagn. 2001 Sep;6(3):169-79. doi: 10.1054/modi.2001.27056. Mol Diagn. 2001. PMID: 11571710

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