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Publications by Frances A. Bu’Lock

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

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Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability

European Journal of Human Genetics
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2018English

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

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Copy Number Variation in Congenital Heart Defects

Current Genetic Medicine Reports
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Recurrence of Congenital Heart Defects in Families

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

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MESP1 Mutations in Patients With Congenital Heart Defects

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Extracardiac Defects in Children With Congenital Heart Disease.

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Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation

American Journal of Human Genetics
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