Birth of a healthy infant after preimplantation genetic diagnosis by sequential blastomere and trophectoderm biopsy for β-thalassemia and HLA genotyping
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference36 articles.
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1. First report on an X-linked hypohidrotic ectodermal dysplasia family with X chromosome inversion: Breakpoint mapping reveals the pathogenic mechanism and preimplantation genetics diagnosis achieves an unaffected birth;Clinica Chimica Acta;2017-12
2. Are there optimal numbers of oocytes, spermatozoa and embryos in assisted reproduction?;JBRA Assisted Reproduction;2016
3. Identification of novel microsatellite markers <1 Mb from theHBBgene and development of a single-tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta-thalassemia;ELECTROPHORESIS;2015-10-05
4. Embryo Genome Profiling by Single-Cell Sequencing for Preimplantation Genetic Diagnosis in a β-Thalassemia Family;Clinical Chemistry;2015-04-01
5. Successful haematopoietic stem cell transplantation in 44 children from healthy siblings conceived after preimplantation HLA matching;Reproductive BioMedicine Online;2014-09
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