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Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

ABSTRACT:

Heterotaxy syndrome is a congenital anomaly syndrome accompanied by thoracic and abdominal situs abnormalities. The study cohort comprises of individuals with heterotaxy or related congenital heart disease (CHD) who have undergone exome sequencing. The purpose of the study is to elucidate the molecular genetics of the disorder as well as contribute to knowledge about the biology of normal and abnormal development of left-right anatomic asymmetry. These results will further help delineate genotype-phenotype associations and provide important information on the causes, management, and prognosis of heterotaxy syndrome.

PROVIDER: phs001814 | dbGaP |

REPOSITORIES: dbGaP

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	GapExchange_phs001814.v1.p1.xml	Xml
	dbGaPEx2.1.5.xsd	Other
	Study_Report.phs001814.Heterotaxy_CHD.v1.p1.MULTI.pdf	Pdf
	manifest_phs001814.Heterotaxy_CHD.v1.p1.c1.GRU.pdf	Pdf
	datadict_v2.xsl	Other

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