Preimplantation genetic diagnosis for α-and β-double thalassemia
Authors:
Open Access
- 11 June 2011
- journal article
- case report
- Published by Springer Nature in Journal of Assisted Reproduction and Genetics
- Vol. 28 (10) , 957-964
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Birth of a healthy infant following preimplantation PKHD1 haplotyping for autosomal recessive polycystic kidney disease using multiple displacement amplificationJournal of Assisted Reproduction and Genetics, 2010
- Singleton birth after preimplantation genetic diagnosis for Huntington disease using whole genome amplificationFertility and Sterility, 2009
- Preimplantation genetic diagnosis for α-thalassaemia in ChinaJournal of Assisted Reproduction and Genetics, 2009
- Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplificationFertility and Sterility, 2009
- Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplificationMolecular Human Reproduction, 2007
- Whole-genome multiple displacement amplification from single cellsNature Protocols, 2006
- Preimplantation genetic diagnosis of Marfan syndrome using multiple displacement amplificationFertility and Sterility, 2006
- Successful preimplantation genetic diagnosis for alpha- and beta-thalassemia in ChinaPrenatal Diagnosis, 2006
- Birth of healthy children after preimplantation diagnosis of β‐thalassemia by whole‐genome amplificationPrenatal Diagnosis, 2003
- An approach to preimplantation diagnosis of β‐thalassaemiaPrenatal Diagnosis, 1991