Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis-Reference-Cited by-同舟云学术

Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis

Published:2002-04 Issue:4 Volume:10 Page:231-238
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Moutou Céline,Gardes Nathalie,Viville Stéphane

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5200794.pdf

Reference29 articles.

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2. Geraedts J, Handyside A, Harper J et al. ESHRE preimplantation genetic diagnosis (PGD) consortium: data collection II (May 2000) Hum Reprod 2000 15: 2673–2683

3. Findlay I, Quirke P, Hall J, Rutherford A . Fluorescent PCR: a new technique for PGD of sex and single-gene defects J Assist Reprod Genet 1996 13: 96–103

4. Sermon K, DeVos A, VandeVelde H et al. Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease) Mol Hum Reprod 1998 4: 791–796

5. Findlay I, Matthews P, Quirke P . Multiple genetic diagnosis from single cells using multiplex PCR: reliability and allele dopout Prenat Diagn 1998 18: 1413–1421

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