Preimplantation genetic diagnosis outcomes and meiotic segregation analysis of robertsonian translocation carriers
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology,Reproductive Medicine
Reference38 articles.
1. Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark;Nielsen;Hum Genet,1991
2. Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis;Scriven;Prenat Diagn,1998
3. Place of preimplantation diagnosis in genetic practice;Kuliev;Am J Med Genet A,2005
4. A proposal for reproductive counseling in carriers of robertsonian translocations: 10 years of experience with preimplantation genetic diagnosis;Keymolen;Hum Reprod,2009
5. Meiotic segregation of robertsonian translocations ascertained in cleavage-stage embryos—implications for preimplantation genetic diagnosis;Bint;Hum Reprod,2011
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1. Chromosome segregation of human non-homologous Robertsonian translocations: insights from preimplantation genetic testing;2024-05-02
2. Preimplantation genetic testing in couples with balanced chromosome rearrangement: a four-year period real world retrospective cohort study;BMC Pregnancy and Childbirth;2024-01-27
3. Does reciprocal translocation affect the meiotic segregation products of non-translocation chromosomes?;Human Fertility;2023-08-08
4. The effect of carrier characteristics and female age on preimplantation genetic testing results of blastocysts from Robertsonian translocation carriers;Journal of Assisted Reproduction and Genetics;2023-06-20
5. Retrospective Analysis of Meiotic Segregation Pattern and Reproductive Outcomes in Blastocysts from Robertsonian Preimplantation Genetic Testing Cycles;Reproductive Sciences;2023-04-26
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