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Paper Details

Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.
Philos Trans R Soc Lond B Biol Sci
26
2016
CHDs, CNV, CNVs, Genomic disorders, PFKP, Patients, X-linked heterotaxy, ZIC3, abdominal situs, congenital heart defects, copy number, copy number variants, cytogenetic abnormalities, d-transposition of the great arteries, heterotaxy, heterotaxy genes, heterotaxy-spectrum CHDs, heterotaxy-spectrum congenital heart defects, human, isolated birth defects, multiple congenital anomaly syndrome, patients, platelet isoform of phosphofructokinase-1, single exon deletion, syndromic conditions
Author NameAffiliation
John W BelmontBaylor College of Medicine
Seema R LalaniBaylor College of Medicine
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