✦ LIBER ✦
A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes
✍ Scribed by Bartholdi, Deborah; Stray-Pedersen, Asbjørg; Azzarello-Burri, Silvia; Kibaek, Maria; Kirchhoff, Maria; Oneda, Beatrice; Rødningen, Olaug; Schmitt-Mechelke, Thomas; Rauch, Anita; Kjaergaard, Susanne
- Book ID
- 121835410
- Publisher
- John Wiley and Sons
- Year
- 2014
- Tongue
- English
- Weight
- 1013 KB
- Volume
- 164
- Category
- Article
- ISSN
- 1552-4825
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