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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 (osteba5-san@euskadi.eus)
Publication Scope
assessment
Countries of Application
Spain
Guideline Publication Status
Published
Languages
Spanish
Authors
OSTEBA (ES)
Publication Year
2004

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