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Genomic Analyses in Cornelia De Lange Syndrome and Related Diagnoses: Novel Candidate Genes, Genotype-Phenotype Correlations and Common Mechanisms.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A(2023)

Cited 10|Views62
Key words
CdLS,cohesin,Cornelia de Lange Syndrome,genome,HDAC8,NIPBL,RAD21,SMC1A,SMC3,transcription
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