Associated Papers
Diagnostic Utility of Whole Genome Sequencing After Negative Karyotyping/Chromosomal Microarray in Infants Born With Multiple Congenital Anomalies.
Yang M et al.
Journal of Korean Medical Science, 2024
HNRNPR Variants that Impair Homeobox Gene Expression Drive Developmental Disorders in Humans.
Duijkers FA et al.
American Journal of Human Genetics, 2019
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