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Paper Details

Further delineation of the SATB2 phenotype.
Eur J Hum Genet
62
2014
2q33, Angelman syndrome, CP, Fragile X syndrome, ID, Rett syndrome, SAS, SATB2, SATB2 gene, SATB2 haploinsufficiency, SATB2-associated syndrome, Satb2, abnormal dentition, c.715C, c.715C>T, children, chromatin remodeling gene, chromosome 2q33, cleft or high-arched palate, cleft palate, crowded, developmental delay, facial dysmorphism, girl, humans, intellectual disability, osteoblast, patient, speech delay
Author NameAffiliation
Max Schubach
Saskia Biskup1] Institute of Clinical Genetics, Germany [3] Hertie Institute for Clinical Brain Research
Deborah BartholdiInstitute of Clinical Genetics
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Release 1.2