Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease-Reference-Cited by-同舟云学术

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Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease

Published:2004-10-01 Issue:10 Volume:10 Page:767-772
ISSN:1460-2407
Container-title:MHR: Basic science of reproductive medicine
language:en
Short-container-title:

Author:

Handyside Alan H.,Robinson Mark D.,Simpson Robert J.,Omar Mark B.,Shaw Marie-Anne,Grudzinskas J.Gedis,Rutherford Anthony

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynaecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

Link

http://academic.oup.com/molehr/article-pdf/10/10/767/3438271/gah101.pdf

Reference27 articles.

1. Ao A, Wells D, Handyside AH et al. (1998) Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli. J Assist Reprod Genet15, 140–144.

2. Dean FB, Hosono S, Fang L et al. (2002) Comprehensive human genome amplification using multiple displacement amplification. Proc Natl Acad Sci USA99, 5261–5266.

3. Dean FB, Nelson JR, Giesler TL et al. (2001) Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification. Genome Res11, 1095–1099.

4. Delhanty JD and Wells D (2002) Preimplantation genetic diagnosis: an alternative to prenatal diagnosis. Expert Rev Mol Diagn2, 395–399.

5. Findlay I, Matthews PL, Mulcahy BK et al. (2001) Using MF-PCR to diagnose multiple defects from single cells: implications for PGD. Mol Cell Endocrinol183 (Supp 1), S5–12.

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