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S1-Leitlinie zum „pränatalen Schnelltest“
Veröffentlicht/Copyright:
8. April 2025
Published Online: 2025-04-08
Published in Print: 2025-04-04
© 2025 Walter de Gruyter GmbH, Berlin/Boston
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Artikel in diesem Heft
- Frontmatter
- MAIN TOPIC The role of genetics in inherited cardiac diseases
- The role of genetics in inherited cardiac diseases
- Current and future diagnostics of congenital heart disease (CHD)
- Understanding inherited cardiomyopathies: clinical aspects and genetic determinants
- Cardiovascular aspects of Noonan syndrome and related disorders
- Cardiac arrhythmias and genetics – current stage
- Advances in human induced pluripotent stem cell (hiPSC)-based disease modelling in cardiogenetics
- Disease mechanism and novel drug therapies for atrial fibrillation
- BERICHTE AUS DER HUMANGENETIK
- Stellungnahmen und Leitlinien
- S1-Leitlinie zum „pränatalen Schnelltest“
- GfH-Verbandsmitteilungen
- Corrigendum to: Long-term experience with gene augmentation therapy in patients with inherited retinal disease associated with biallelic mutations in RPE65
Artikel in diesem Heft
- Frontmatter
- MAIN TOPIC The role of genetics in inherited cardiac diseases
- The role of genetics in inherited cardiac diseases
- Current and future diagnostics of congenital heart disease (CHD)
- Understanding inherited cardiomyopathies: clinical aspects and genetic determinants
- Cardiovascular aspects of Noonan syndrome and related disorders
- Cardiac arrhythmias and genetics – current stage
- Advances in human induced pluripotent stem cell (hiPSC)-based disease modelling in cardiogenetics
- Disease mechanism and novel drug therapies for atrial fibrillation
- BERICHTE AUS DER HUMANGENETIK
- Stellungnahmen und Leitlinien
- S1-Leitlinie zum „pränatalen Schnelltest“
- GfH-Verbandsmitteilungen
- Corrigendum to: Long-term experience with gene augmentation therapy in patients with inherited retinal disease associated with biallelic mutations in RPE65