bibliographic entry 7010771 [be/7010771]
https://w3id.org/oc/corpus/be/7010771

is a

• bibliographic reference

content

• Writzl, K, Knegt, A. C. (2013). 6p21.3 microdeletion involving the SYNGAP1 gene in a patient with intellectual disability, seizures and severe speech impairment. Am. J. Med. Genet. A. 161A, 1682–1685. DOI: 10.1002/ajmg.a.35930 PMID: 23687080

references

• https://w3id.org/oc/corpus/br/5692840