Preimplantation genetic diagnosis of hemophilia A-Reference-Cited by-同舟云学术

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Preimplantation genetic diagnosis of hemophilia A

Published:2016-10 Issue:S1 Volume:14 Page:
ISSN:1477-9560
Container-title:Thrombosis Journal
language:en
Short-container-title:Thrombosis J

Author:

Chen Ming,Chang Shun-Ping,Ma Gwo-Chin,Lin Wen-Hsian,Chen Hsin-Fu,Chen Shee-Uan,Tsai Horng-Der,Tsai Feng-Po,Shen Ming-Ching

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Link

http://link.springer.com/content/pdf/10.1186/s12959-016-0098-9.pdf

Reference41 articles.

1. Handyside A, Kontogianni EH, Hardy K, Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature. 1990;344:768–70.

2. Brezina PR, Brezina DS, Kearns WG. Preimplantation genetic testing. BMJ. 2012;345:e5908.

3. Harton GL, De Rycke M, Fiorentino F, Moutou C, SenGupta S, Traeger-Synodinos J, et al. European Society for Human Reproduction and Embryology (ESHRE) PGD Consortium: ESHRE PGD consortium best practice guidelines for amplification-based PGD. Human Reprod. 2011;26:33–40.

4. Chen HF, Chang SP, Wu SH, Lin WH, Lee YC, Ni YH, et al. Validating a rapid, real-time, PCR-based direct mutation detection assay for preimplantation genetic diagnosis. Gene. 2014;548:299–305.

5. Kuo SJ, Ma GC, Chang SP, Wu HH, Chen CP, Chang TM, et al. Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification-refractory mutation system-quantitative polymerase chain reaction. Taiwan J Obstet Gynecol. 2011;50:468–73.

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic counseling for pre-implantation genetic testing of monogenic disorders (PGT-M);Frontiers in Reproductive Health;2023-12-15

2. Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future Directions;International Journal of Molecular Sciences;2023-07-24

3. Hemophilia A (Factor VIII Deficiency);Hematology/Oncology Clinics of North America;2021-12

4. Genetic Counseling: Preconception, Prenatal, and Perinatal;Genetic Disorders and the Fetus;2021-04-20

5. Case Report: Identification of a de novo Missense Mutation in the F8 Gene, p.(Phe690Leu)/c.2070C > A, Causing Hemophilia A: A Case Report;Frontiers in Genetics;2021-03-05

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