Gabriel Dworschak
0000-0003-0015-6964
5 papers found
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Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder
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