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Article

Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal Defects

1 Apr 2003

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12632326
DOI: 10.1086/374319

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Related research

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Research trail→

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Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal DefectsPMID 12632326Read ↗

Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome.Semantic proximity Read ↗

Novel CRELD1 gene mutations in patients with atrioventricular septal defect.Semantic proximity Read ↗

Human Genetics of Atrioventricular Septal Defect.Semantic proximity Read ↗

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.Semantic proximity Read ↗

Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformationsSemantic proximity Read ↗

A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India.Semantic proximity Read ↗

Human Genetics of Atrial Septal Defect.Semantic proximity Read ↗

Novel Autosomal Recessive Splice-Altering Variant in PRKD1 Is Associated with Congenital Heart DiseaseSemantic proximity Read ↗

Molecular genetics of atrioventricular septal defects.Semantic proximity Read ↗

High-risk genes involved in common septal defects of congenital heart diseaseSemantic proximity Read ↗

Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect.Semantic proximity Read ↗

Characterisation of a novel cardiac phenotype in patients with GFPT1 or DPAGT1 mutationsSemantic proximity Read ↗

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