bibliographic entry 6789755 [be/6789755]
https://w3id.org/oc/corpus/be/6789755

is a

• bibliographic reference

content

• Cusmano-Ozog, K, Manning, MA, Hoyme, HE. 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay, Am J Med Genet C Semin Med Genet, 2007, 145C, 4, 393, 8, DOI: 10.1002/ajmg.c.30155, PMID: 17926345

references

• https://w3id.org/oc/corpus/br/5212017