bibliographic entry 12414126 [be/12414126]
https://w3id.org/oc/corpus/be/12414126

is a

• bibliographic reference

content

• Muenke, M, Gripp, KW, McDonald-McGinn, DM, Gaudenz, K, Whitaker, LA, Bartlett, SP, Wilkie, AO. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome, American journal of human genetics, 1997, 60, 3, 555, 564, PMID: 9042914

references

• https://w3id.org/oc/corpus/br/1744806