Live births following karyomapping – a “key” milestone in the development of preimplantation genetic diagnosis
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology
Reference13 articles.
1. Genetic analysis of DNA from single human oocytes: a model for preimplantation diagnosis of cystic fibrosis;Coutelle;BMJ,1989
2. Development and clinical application of a strategy for preimplantation genetic diagnosis of single gene disorders combined with HLA matching;Fiorentino;Mol. Hum. Reprod,2004
3. Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis [see comments];Handyside;N. Engl. J. Med,1992
4. Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease;Handyside;Mol. Hum. Reprod,2004
5. Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes;Handyside;J. Med. Genet,2010
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