A new enrichment approach for candidate gene detection in unexplained recurrent pregnancy loss and implantation failure
Author:
Funder
Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00438-022-01972-5.pdf
Reference77 articles.
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2. Assou S, Boumela I, Haouzi D et al (2012) Transcriptome analysis during human trophectoderm specification suggests new roles of metabolic and epigenetic genes. PLoS ONE 7:e39306. https://doi.org/10.1371/journal.pone.0039306
3. Atasever M, Soyman Z, Demirel E et al (2016) Diminished ovarian reserve: is it a neglected cause in the assessment of recurrent miscarriage? A cohort study. Fertil Steril 105:1236–1240. https://doi.org/10.1016/j.fertnstert.2016.01.001
4. Avbelj Stefanija M, Jeanpierre M, Sykiotis GP et al (2012) An ancient founder mutation in PROKR2 impairs human reproduction. Hum Mol Genet 21:4314–4324. https://doi.org/10.1093/hmg/dds264
5. Bajnóczky K, Gardó S (1993) “Premature anaphase” in a couple with recurrent miscarriages. Hum Genet 92:388–390. https://doi.org/10.1007/BF01247341
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