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Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case

โœ Scribed by Minor, Agata; Shinawi, Marwan; Hogue, Jacob S.; Vineyard, Marisa; Hamlin, Damara R.; Tan, Christopher; Donato, Kirsten; Wysinger, Latrice; Botes, Shaun; Das, Soma; del Gaudio, Daniela


Book ID
122282113
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
629 KB
Volume
537
Category
Article
ISSN
0378-1119

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