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SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis
Author(s) -
Hailong Huang,
Meiying Cai,
Yan Wang,
Bin Liang,
Na Lin,
Liangpu Xu
Publication year - 2021
Publication title -
risk management and healthcare policy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.828
H-Index - 22
ISSN - 1179-1594
DOI - 10.2147/rmhp.s286001
Subject(s) - fetal echocardiography , snp array , fetus , prenatal diagnosis , medicine , heart disease , snp , copy number variation , karyotype , pregnancy , obstetrics , biology , chromosome , single nucleotide polymorphism , genetics , genotype , genome , gene
This study aimed to examine the effectiveness of the SNP array for the prenatal diagnosis of congenital heart disease (CHD) screened by echocardiography.

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