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Publications by Fanny Kortüm
Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability
European Journal of Human Genetics
Genetics
Related publications
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
American Journal of Human Genetics
Genetics
Brachydactyly-Mesomelia-Intellectual Disability-Heart Defects Syndrome
Dosage Changes of MED13L Further Delineate Its Role in Congenital Heart Defects and Intellectual Disability
European Journal of Human Genetics
Genetics
TBX1 Loss‑of‑function Mutation Contributes to Congenital Conotruncal Defects
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Vulnerability of the Developing Heart to Oxygen Deprivation as a Cause of Congenital Heart Defects
Journal of the American Heart Association
Cardiovascular Medicine
Cardiology
Recurrence of Congenital Heart Defects in Families
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Evaluation of Heterogeneity in the Association Between Congenital Heart Defects and Variants of Folate Metabolism Genes: Conotruncal and Left-Sided Cardiac Defects
Birth Defects Research Part A - Clinical and Molecular Teratology
Child Health
Pediatrics
Perinatology
Medicine
Developmental Biology
Embryology
EP06.02: The Landscape of Pathogenic Copy Number Variants in Fetuses With Congenital Heart Defects
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
Comprehensive Approach to Congenital Heart Defects
Journal of Cardiovascular Disease Research
Cardiovascular Medicine
Cardiology
