Author:
Massin N.,Gougeon A.,Meduri G.,Thibaud E.,Laborde K.,Matuchansky C.,Constancis E.,Vacher-Lavenu M.C.,Paniel B.,Zorn J.R.,Misrahi M.,Kuttenn F.,Touraine Ph.
Publisher
Oxford University Press (OUP)
Subject
Obstetrics and Gynaecology,Rehabilitation,Reproductive Medicine
Reference25 articles.
1. Aittomaki K, Dieguez Lucena JL, Pakarinen P, Sistoneen P, Tapanainen J, Gromol J, Kaskikari R, Sankila EM, Lehvaslaiho H, Reyes Engel A et al. (1995) Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell82, 959–968.
2. Aittomaki K, Herva R, Stenman UH, Juntunen K, Ylostalo P, Hovatta O and de la Chapelle A (1996) Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene. J Clin Endocrinol Metab81, 3722–3726.
3. Allen LA, Achermann JC, Pakarinen P, Kotlar TJ, Huhtaniemi IT, Jameson JL, Cheetham TD and Ball SG (2003) A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics. Hum Reprod18, 251–256.
4. Anasti JN (1998) Premature ovarian failure: an update. Fertil Steril70, 1–15.
5. Beau I, Touraine P, Meduri G, Gougeon A, Desroches A, Matuchansky C, Milgrom E, Kuttenn F and Misrahi M (1998) A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor. J Clin Invest102, 1352–1359.
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