Trent RJ - Search Results

1

Computer-assisted reading of DNA sequences.

Le H, Hinchcliffe M, Yu B, Trent RJ. Le H, et al. Among authors: trent rj. Methods Mol Med. 2008;141:177-97. doi: 10.1007/978-1-60327-148-6_10. Methods Mol Med. 2008. PMID: 18453090

2

Challenges for clinical genetic DNA testing.

Trent RJ, Yu B, Caramins M. Trent RJ, et al. Expert Rev Mol Diagn. 2004 Mar;4(2):201-8. doi: 10.1586/14737159.4.2.201. Expert Rev Mol Diagn. 2004. PMID: 14995906 Review.

3

Complex phenotypes in the haemoglobinopathies: recommendations on screening and DNA testing.

Trent RJ, Webster B, Bowden DK, Gilbert A, Holl PJ, Lindeman R, Lammi A, Rowell J, Hinchcliffe M, Colley A, Wilson M, Saleh M, Blackwell J, Petrou V. Trent RJ, et al. Pathology. 2006 Dec;38(6):507-19. doi: 10.1080/00313020601027634. Pathology. 2006. PMID: 17393977 Review.

4

Diagnostic validation of a familial hypercholesterolaemia cohort provides a model for using targeted next generation DNA sequencing in the clinical setting.

Hinchcliffe M, Le H, Fimmel A, Molloy L, Freeman L, Sullivan D, Trent RJ. Hinchcliffe M, et al. Among authors: trent rj. Pathology. 2014 Jan;46(1):60-8. doi: 10.1097/PAT.0000000000000026. Pathology. 2014. PMID: 24300713

5

DNA testing in familial hypertrophic cardiomyopathy: clinical and laboratory implications.

Smart RV, Yu B, Le H, French JA, Richmond DR, Jeremy RW, Semsarian C, Cheung L, Ross DA, Trent RJ. Smart RV, et al. Among authors: trent rj. Clin Genet. 1996 Oct;50(4):169-75. doi: 10.1111/j.1399-0004.1996.tb02621.x. Clin Genet. 1996. PMID: 9001794

6

Applications of capillary electrophoresis in DNA mutation analysis of genetic disorders.

Le H, Fung D, Trent RJ. Le H, et al. Among authors: trent rj. Mol Pathol. 1997 Oct;50(5):261-5. doi: 10.1136/mp.50.5.261. Mol Pathol. 1997. PMID: 9497917 Free PMC article.

7

Prenatal diagnosis for thalassaemia in a multicultural society.

Trent RJ, Le H, Yu B. Trent RJ, et al. Prenat Diagn. 1998 Jun;18(6):591-8. Prenat Diagn. 1998. PMID: 9664605

8

Capillary electrophoresis: new technology for DNA diagnostics.

Le H, Fung DC, Yu B, Trent RJ. Le H, et al. Among authors: trent rj. Pathology. 1998 Aug;30(3):304-8. doi: 10.1080/00313029800169496. Pathology. 1998. PMID: 9770198

9

DNA testing for haemochromatosis: diagnostic, predictive and screening implications.

Trent RJ, Le H, Yu B, Young G, Bowden DK. Trent RJ, et al. Pathology. 2000 Nov;32(4):274-9. Pathology. 2000. PMID: 11186424

10

A polymorphism in the poliovirus receptor gene differs in motor neuron disease.

Saunderson R, Yu B, Trent RJ, Pamphlett R. Saunderson R, et al. Among authors: trent rj. Neuroreport. 2004 Feb 9;15(2):383-6. doi: 10.1097/00001756-200402090-00034. Neuroreport. 2004. PMID: 15076773

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