Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/1097-0223(200007)20:7<599::AID-PD883>3.0.CO;2-Q/fullpdf
Reference24 articles.
1. Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization;Blanco;Hum Reprod,1996
2. FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13);Blanco;Cytogenet Cell Genet,1998
3. Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions;Conn;Hum Genet,1998
4. Cytogenetic studies in male infertility: a review;De Braekeleer;Hum Reprod,1991
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1. Reproductive outcomes after pre‐implantation genetic testing in heterozygous Robertsonian translocation carriers: A retrospective cohort study of 144 cycles;International Journal of Gynecology & Obstetrics;2023-03-13
2. How much, if anything, do we know about sperm chromosomes of Robertsonian translocation carriers?;Cellular and Molecular Life Sciences;2020-06-08
3. Interchromosomal effect in carriers of translocations and inversions assessed by preimplantation genetic testing for structural rearrangements (PGT-SR);Journal of Assisted Reproduction and Genetics;2019-11-06
4. Decrease of spermatozoa with an unbalanced chromosome content after cell sorting in men carrying a structural chromosomal abnormality;Andrology;2019-05-22
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