Associated Papers
Molecular mechanism, diagnosis, and treatment of VACTERL association.
Sun M et al.
Frontiers in Pediatrics, 2025
Real-world performance analysis of a novel computational method in the precision oncology of pediatric tumors.
Vodicska B et al.
World Journal of Pediatrics : Wjp, 2023
36914906 (PubMed )
Supplement: 12519_2023_700_MOESM1_ESM.xlsx › Driver_list
Benefits and outcomes of a new multidisciplinary approach for the management and financing of sudden unexplained death cases in a forensic setting in Switzerland.
Neubauer J et al.
Forensic Science International, 2022
Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.
Hildebrandt MR et al.
Stem Cell Reports, 2019
31813827 (PubMed )
Supplement: mmc3.xlsx › SNVs
A review of genetic factors contributing to the etiopathogenesis of anorectal malformations.
Khanna K et al.
Pediatric Surgery International, 2018
Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
Paulussen AD et al.
European Journal of Human Genetics : Ejhg, 2016
Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.
Reutter H et al.
Pediatric Nephrology (berlin, Germany), 2016
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.
Hilger AC et al.
Human Mutation, 2015
Genetic basis of human left-right asymmetry disorders.
Deng H et al.
Expert Reviews in Molecular Medicine, 2015
Genetic and functional analyses of ZIC3 variants in congenital heart disease.
Cowan J et al.
Human Mutation, 2014
The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle.
D'Alessandro LC et al.
American Journal of Medical Genetics. Part A, 2013
Familial transposition of the great arteries caused by multiple mutations in laterality genes.
De Luca A et al.
Heart (british Cardiac Society), 2010
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