Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome - Concepedia

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Publication | Open Access

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

DOI Full Paper Access

96

Citations

20

References

2011

Year

Kemal O. Yariz, Tom Walsh, Michail Spiliopoulos, Duygu Duman, Göğşen Önalan, Mary‐Claire King, Mustafa Tekin

Fertility and Sterility

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsReceptor BiologyEmpty Follicle SyndromeEndocrinologyMedicineHormone/choriogonadotropin Receptor

References

	Year	Citations

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