Diagnóstico preimplantacional de portadores de cromosoma X frágil y otros trastornos hereditarios en técnicas de fecundación artificial (Informe nº: Osteba D-05-01)
- 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)
- Guideline Contact
- Marta Lopez de Argumedo ([email protected])
- English Title Translation
- PREIMPLANTATIONAL DIAGNOSIS OF FRAGILE CHROMOSOME X CARRIERS AND OTHER HEREDITARY DISORDERS IN ARTIFICIAL FERTILISATION TECHNIQUES
- Publication Scope
- assessment
- Countries of Application
- Spain
- Guideline Publication Status
- Published
- Languages
- Spanish
- Authors
- OSTEBA (ES)
- Publication Year
- 2004
