Concepedia

Genetic abnormalities in Turkish women with premature ovarian failure

Gülay Ceylaner, Sündüz Özlem Altınkaya, Leyla Mollamahmutoğlu, Serdar Ceylaner

International Journal of Gynecology & Obstetrics · 2010 · 34 citations · 20 references

DOI

Abstract

A genetic cause of POF was identified in 39 (52%) of 75 patients. A thorough genetic evaluation of women with POF should be performed regardless of clinical features suggestive of chromosomal abnormality.

References

20

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

Kristiina Aittomäki, JoséLuis Dieguez Lucena, Pirjo Pakarinen et al. · Cell · 1995 · 979 citations · Full text

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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Laura Crisponi, Manila Deiana, Angela Loi et al. · Nature Genetics · 2001 · 974 citations

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Hypergonadotropic Ovarian Failure Associated with an Inherited Mutation of Human Bone Morphogenetic Protein-15 (BMP15) Gene

Elisa Di Pasquale, Paolo Beck‐Peccoz, Luca Persani · The American Journal of Human Genetics · 2004 · 502 citations · Full text

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Family history as a predictor of early menopause

Daniel W. Cramer, Huijuan Xu, Bernard L. Harlow · Fertility and Sterility · 1995 · 240 citations

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Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations

Anne Fogli, Diana Rodriguez, Éléonore Eymard-Pierre et al. · The American Journal of Human Genetics · 2003 · 193 citations · Full text

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