P24 Preimplantation genetic diagnosis for cystic fibrosis: The Montpellier center experience
✍ Scribed by C. Fernandez; C. Guittard; M. Des Georges; C. Coubes; T. Anahory; H. Déchaud; S. Hamamah; M. Claustres; A. Girardet
- Book ID
- 119611620
- Publisher
- Reproductive Healthcare Ltd
- Year
- 2010
- Tongue
- English
- Weight
- 64 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1472-6491
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Preimplantation genetic diagnosis (PGD) was attempted in 12 couples in whom both parents carry the common AF508 deletion causing cystic fibrosis (CF). In vitro fertilization (IVF) was followed by cleavage stage biopsy on days 2 and 3 and removal of one or two cells for genetic analysis by nested pol
Cystic fibrosis (CF) is an autosomal recessive disease characterized by obstruction and chronic infections of the respiratory tract and pancreatic insufficiency. The gene was cloned in 1989 and the most frequent mutation was shown to be the delta F508 mutation. During PGD, embryos obtained in vitro