Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier

BACKGROUND: Ring chromosomes are normally associated with developmental anomalies and are rarely inherited. An exception to this rule is provided by deletion/ring cases. We were provided with a unique opportunity to investigate the meiotic segregation at oogenesis in a woman who is a carrier of a de...

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Detalles Bibliográficos
Autores principales: Mantzouratou, Anna, Mania, Anastasia, Apergi, Marianna, Laver, Sarah, Serhal, Paul, Delhanty, JDA
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637284/
https://www.ncbi.nlm.nih.gov/pubmed/19166580
http://dx.doi.org/10.1186/1755-8166-2-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637284/
https://www.ncbi.nlm.nih.gov/pubmed/19166580
http://dx.doi.org/10.1186/1755-8166-2-3

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