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Preimplantation genetic diagnosis for α-thalassaemia in China
PURPOSE: To report the usage of PGD for α-thalassaemia with the - -(SEA) genotype. METHOD: A PGD protocol using fluorescent gap PCR was performed for 51 cycles on 43 couples with the - -(SEA) genotype. Allele drop-out and amplification failure rates were retrospectively analyzed. RESULTS: A total of...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer US
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758951/ https://www.ncbi.nlm.nih.gov/pubmed/19813097 http://dx.doi.org/10.1007/s10815-009-9336-4 |
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author | Xu, Yan-Wen Zeng, Yan-Hong Deng, Jie Liu, Ying Gao, Ling Zhou, Can-Quan Zhuang, Guang-Lun |
author_facet | Xu, Yan-Wen Zeng, Yan-Hong Deng, Jie Liu, Ying Gao, Ling Zhou, Can-Quan Zhuang, Guang-Lun |
author_sort | Xu, Yan-Wen |
collection | PubMed |
description | PURPOSE: To report the usage of PGD for α-thalassaemia with the - -(SEA) genotype. METHOD: A PGD protocol using fluorescent gap PCR was performed for 51 cycles on 43 couples with the - -(SEA) genotype. Allele drop-out and amplification failure rates were retrospectively analyzed. RESULTS: A total of 472 embryos were biopsied. Amplification was achieved in 390 blastomeres, accounting for an amplification rate of 82.6%. In total, 120 wild-type, 94 heterozygotes and 140 homozygous mutant embryos were diagnosed. The successful diagnosis rate was 75.0%. The ADO rate in 49 blastomeres from six donated embryos was 16.4%. One hundred and fifty four embryos were transferred, resulting in 25 clinical pregnancies with an implantation rate of 24.0%. CONCLUSIONS: Single-round fluorescent gap PCR is a feasible and effective strategy in the PGD for α-thalassaemia with the - -(SEA) genotype. |
format | Text |
id | pubmed-2758951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-27589512009-10-15 Preimplantation genetic diagnosis for α-thalassaemia in China Xu, Yan-Wen Zeng, Yan-Hong Deng, Jie Liu, Ying Gao, Ling Zhou, Can-Quan Zhuang, Guang-Lun J Assist Reprod Genet Original Paper PURPOSE: To report the usage of PGD for α-thalassaemia with the - -(SEA) genotype. METHOD: A PGD protocol using fluorescent gap PCR was performed for 51 cycles on 43 couples with the - -(SEA) genotype. Allele drop-out and amplification failure rates were retrospectively analyzed. RESULTS: A total of 472 embryos were biopsied. Amplification was achieved in 390 blastomeres, accounting for an amplification rate of 82.6%. In total, 120 wild-type, 94 heterozygotes and 140 homozygous mutant embryos were diagnosed. The successful diagnosis rate was 75.0%. The ADO rate in 49 blastomeres from six donated embryos was 16.4%. One hundred and fifty four embryos were transferred, resulting in 25 clinical pregnancies with an implantation rate of 24.0%. CONCLUSIONS: Single-round fluorescent gap PCR is a feasible and effective strategy in the PGD for α-thalassaemia with the - -(SEA) genotype. Springer US 2009-10-08 2009-07 /pmc/articles/PMC2758951/ /pubmed/19813097 http://dx.doi.org/10.1007/s10815-009-9336-4 Text en © The Author(s) 2009 |
spellingShingle | Original Paper Xu, Yan-Wen Zeng, Yan-Hong Deng, Jie Liu, Ying Gao, Ling Zhou, Can-Quan Zhuang, Guang-Lun Preimplantation genetic diagnosis for α-thalassaemia in China |
title | Preimplantation genetic diagnosis for α-thalassaemia in China |
title_full | Preimplantation genetic diagnosis for α-thalassaemia in China |
title_fullStr | Preimplantation genetic diagnosis for α-thalassaemia in China |
title_full_unstemmed | Preimplantation genetic diagnosis for α-thalassaemia in China |
title_short | Preimplantation genetic diagnosis for α-thalassaemia in China |
title_sort | preimplantation genetic diagnosis for α-thalassaemia in china |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758951/ https://www.ncbi.nlm.nih.gov/pubmed/19813097 http://dx.doi.org/10.1007/s10815-009-9336-4 |
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