A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes
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A. Stray-Pedersen | A. Rauch | S. Kjaergaard | M. Kirchhoff | D. Bartholdi | O. Rødningen | B. Oneda | M. Kibaek | T. Schmitt-Mechelke | S. Azzarello-Burri