bibliographic entry 12414133 [be/12414133]
https://w3id.org/oc/corpus/be/12414133

is a

• bibliographic reference

content

• Dodé, C, Levilliers, J, Dupont, J-M, De Paepe, A, Le Dû, N, Soussi-Yanicostas, N, Hardelin, J-P. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome, Nature Genetics, 2003, 33, 4, 463, 465, DOI: 10.1038/ng1122, PMID: 12627230

references

• https://w3id.org/oc/corpus/br/3173608