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Assessment of the national newborn screening programme for permanent hearing loss. Screening strategy and test performance

Public Health guideline - Posted on 23/6/2025

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Tests based on cell-free DNA in the context of screening for trisomy 21: appropriateness of detecting other chromosomal abnormalities

Public Health guideline - Posted on 2/10/2024 - Mis à jour le 28/10/2024

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Newborn screening for spinal muscular atrophy_Advance assessment of extension of screening to the general population in France

Public Health guideline - Posted on 10/7/2024

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Clinical and economic assessment of screening for HFE1 haemochromatosis in 2004

Public Health guideline - Posted on 1/4/2004 - Mis à jour le 12/12/2006

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See 4 result in Practice Guidelines and Other Guides

Next-generation sequencing of targeted gene panels in the diagnosis of hereditary cardiomyopathies - INAHTA Brief

Health technology assessment - Posted on 28/2/2025 - Mis à jour le 3/12/2025

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Comparative genomic hybridization array (CGHA) analysis in postnatal context - INAHTA Brief

Health technology assessment - Posted on 20/7/2023

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Nasal nitric oxide (NO) measurement as a diagnostic test for primary ciliary dyskinesia (PCD) - INAHTA Brief

Health technology assessment - Posted on 16/9/2020

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