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    The library contains links to guidelines published or endorsed by GIN member organisations from across the globe. It also contains a registry of planned guidelines and guidelines in development. Non members are actively encouraged to register their guidelines in development. Contact [email protected] to find out how. To learn more about GIN and membership, click the website button above.

    Diagnóstico preimplantacional de portadores de cromosoma X frágil y otros trastornos hereditarios en técnicas de fecundación artificial (Informe nº: Osteba D-05-01)

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    Collection
    Guidelines International Network
    MeSH Terms
    Chromosome Disorders (C16.131.260); X Chromosome (A11.284.187.865.982); Congenital; Hereditary; and Neonatal Diseases and Abnormalities (C16); Genetic Diseases; X-Linked (C16.320.322); Genetic Diseases; Inborn (C16.320); Diagnostic Techniques and Procedures (E01.370); Reproduction (G08.686.785.760)
    English Title Translation
    PREIMPLANTATIONAL DIAGNOSIS OF FRAGILE CHROMOSOME X CARRIERS AND OTHER HEREDITARY DISORDERS IN ARTIFICIAL FERTILISATION TECHNIQUES
    Record Publish Year
    2020
    Guideline Contact
    Marta Lopez de Argumedo ([email protected])
    Publication Scope
    assessment
    Countries of Application
    Spain
    Guideline Publication Status
    Published
    Languages
    Spanish
    Authors
    OSTEBA (ES)
    Publication Year
    2004

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