Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes - Concepedia

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Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

197

Citations

33

References

2006

Year

Nelly Pitteloud, Astrid U. Meysing, Richard Quinton, James S. Acierno, Andrew Dwyer, Lacey Plummer, Eric Fliers, Paul A. Boepple, Frances J. Hayes, Stephanie B. Seminara,

Molecular and Cellular Endocrinology

FibrosisDevelopmental BiologyMendelian DisorderCell DivisionReproductive PhenotypesGenetic DisorderGeneticsPathologyWide SpectrumCell DevelopmentCause Kallmann SyndromeFibroblast Growth FactorMedicineDisorders Of Sex DevelopmentEmbryology

References

	Year	Citations

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