Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation ΔF508 by fluorescent polymerase chain reaction [1]

Prenatal Diagnosis

Volumn 19, Issue 13, 1999, Pages 1248-1250

  Moutou, Céline ^a   Viville, Stéphane ^b,c  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^b INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^c SIHCUS CMCO Centre Medico Chirurgical et Obstetrical   (France)

Author keywords

[No Author keywords available]

Indexed keywords

FLUOROCHROME;

CONTROLLED STUDY; CYSTIC FIBROSIS; DIAGNOSTIC ACCURACY; EMBRYO; GENE MUTATION; HUMAN CELL; LETTER; LYMPHOBLAST; NONHUMAN; POLYMERASE CHAIN REACTION; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL;

CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; HUMANS; POLYMERASE CHAIN REACTION; PREGNANCY; PREIMPLANTATION DIAGNOSIS;

EID: 0033378281     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199912)19:13<1248::AID-PD737>3.0.CO;2-G     Document Type: Letter

References (9)

1. Findlay I, Ray P, Quirke P, Rutherford A, Lilford R. 1995a. Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis. Hum Reprod 10: 1609-1618.
2. Findlay I, Urquhart A, Quirke P, Sullivan K, Rutherford AJ, Lilford RJ. 1995b. Simultaneous DNA 'fingerprinting', diagnosis of sex and single-gene defect status from single cells. Hum Reprod 10: 1005-1013.
3. Handyside AH. 1998. Clinical evaluation of preimplantation genetic diagnosis. Prenat Diagn 18: 1345-1348.
4. Handyside AH, Scriven PN, Ogilvie CM. 1998. The future of preimplantation genetic diagnosis. Hum Reprod 13 (Suppl. 4): 249-255.
5. Lissens W, Sermon K. 1997. Preimplantation genetic diagnosis: current status and new developments. Hum Reprod 12: 1756-1761.
6. Sermon K, DeVos A, VandeVelde H, Seneca S, Lissens W, Joris H, Vandervorst M, VanSteirteghem A, Liebaers I. 1998a. Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease). Mol Hum Reprod 4: 791-796.
7. Sermon K, Goossens V, Seneca S, Lissens W, De Vos A, Vandervorst M, Van Steirteghem A, Liebaers I. 1998b. Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos. Prenat Diagn 18: 1427-1436.
8. Sherlock J, Cirigliano V, Petrou M, Tutschek B, Adinolfi M. 1998. Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells. Ann Hum Genet 62: 9-23.
9. Wells D, Sherlock JK. 1998. Strategies for preimplantation genetic diagnosis of single gene disorders by DNA amplification. Prenat Diagn 18: 1389-1401.