Collection
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 (osteba5-san@euskadi.eus)
English Title Translation
PREIMPLANTATIONAL DIAGNOSIS OF FRAGILE CHROMOSOME X CARRIERS AND OTHER HEREDITARY DISORDERS IN ARTIFICIAL FERTILISATION TECHNIQUES
Record Publish Year
2004
Publication Scope
assessment
Countries of Application
Spain
Guideline Publication Status
Published
Languages
Spanish
Authors
OSTEBA (ES)
Publication Year
2004