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Publications by Lisa C.A. D’Alessandro

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

American Journal of Human Genetics
Genetics
2014English

Related publications

Rare Copy Number Variants Analysis Identifies Novel Candidate Genes in Heterotaxy Syndrome Patients With Congenital Heart Defects

Genome Medicine
Molecular MedicineGeneticsMolecular Biology
2018English

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
2018English

EP06.02: The Landscape of Pathogenic Copy Number Variants in Fetuses With Congenital Heart Defects

Ultrasound in Obstetrics and Gynecology
Nuclear MedicineRadiologyUltrasound TechnologyGynecologyReproductive MedicineRadiologicalImagingObstetricsMedicine
2017English

Copy Number Variation in Congenital Heart Defects

Current Genetic Medicine Reports
2014English

Recurrence of Congenital Heart Defects in Families

Circulation
Cardiovascular MedicinePhysiologyCardiology
2009English

Vulnerability of the Developing Heart to Oxygen Deprivation as a Cause of Congenital Heart Defects

Journal of the American Heart Association
Cardiovascular MedicineCardiology
2014English

MESP1 Mutations in Patients With Congenital Heart Defects

Human Mutation
Genetics
2016English

Extracardiac Defects in Children With Congenital Heart Disease.

Heart
Cardiovascular MedicineCardiology
1979English

Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation

American Journal of Human Genetics
Genetics
2018English

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