DOI: 10.1093/hmg/7.9.1475. Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

10.1093/hmg/7.9.1475

Crossref journal-article

Oxford University Press (OUP)

Human Molecular Genetics (286)

Bibliography

Anderson, J. (1998). Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand. Human Molecular Genetics, 7(9), 1475â1483.

Authors 1

J Anderson (first)

References 0 Referenced 205

None

Dates

Type	When
Created	23 years ago (July 26, 2002, 6:20 p.m.)
Deposited	8 years ago (Aug. 23, 2017, 4:42 a.m.)
Indexed	3 weeks ago (Aug. 3, 2025, 6:55 p.m.)
Issued	26 years, 11 months ago (Sept. 1, 1998)
Published	26 years, 11 months ago (Sept. 1, 1998)
Published Print	26 years, 11 months ago (Sept. 1, 1998)

Funders 0

None

BibTeX

@article{Anderson_1998, title={Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand}, volume={7}, ISSN={1460-2083}, url={http://dx.doi.org/10.1093/hmg/7.9.1475}, DOI={10.1093/hmg/7.9.1475}, number={9}, journal={Human Molecular Genetics}, publisher={Oxford University Press (OUP)}, author={Anderson, J}, year={1998}, month=sep, pages={1475–1483} }

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