Delineation of phenotypes and genotypes related to cohesin structural protein RAD21

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3.- Delineation_RAD21.pdf (1.02 MB)
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URI: http://hdl.handle.net/10641/2008
ISSN: 1432-1203
DOI: 10.1007/s00439-020-02138-2

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2020

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Human Genetics
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RAD21, NIPBL, SMC1A, Cohesinopathy, Cornelia de Lange syndrome, Mungan syndrome, Genotype-phenotype correlation

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