DeborahD.BartholdiDeborahD., AsbjørgA.Stray-PedersenAsbjørgA., SilviaS.Azzarello-BurriSilviaS., MariaM.KibaekMariaM., MariaM.KirchhoffMariaM., A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes, „American Journal of Medical Genetics. Part A”, 164A (5), 2014, s. 1277–1283, DOI:10.1002/ajmg.a.36439, ISSN1552-4833, PMID:24664804 [dostęp 2017-02-02].
DeborahD.BartholdiDeborahD., AsbjørgA.Stray-PedersenAsbjørgA., SilviaS.Azzarello-BurriSilviaS., MariaM.KibaekMariaM., MariaM.KirchhoffMariaM., A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes, „American Journal of Medical Genetics. Part A”, 164A (5), 2014, s. 1277–1283, DOI:10.1002/ajmg.a.36439, ISSN1552-4833, PMID:24664804 [dostęp 2017-02-02].
DeborahD.BartholdiDeborahD., AsbjørgA.Stray-PedersenAsbjørgA., SilviaS.Azzarello-BurriSilviaS., MariaM.KibaekMariaM., MariaM.KirchhoffMariaM., A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes, „American Journal of Medical Genetics. Part A”, 164A (5), 2014, s. 1277–1283, DOI:10.1002/ajmg.a.36439, ISSN1552-4833, PMID:24664804 [dostęp 2017-02-02].