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Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure.
Aittomäki K, Lucena JL, Pakarinen P, Sistonen P, Tapanainen J, Gromoll J, Kaskikari R, Sankila EM, Lehväslaiho H, Engel AR, Nieschlag E, Huhtaniemi I, de la Chapelle A. Aittomäki K, et al. Among authors: Gromoll J. Cell. 1995 Sep 22;82(6):959-68. doi: 10.1016/0092-8674(95)90275-9. Cell. 1995. PMID: 7553856
Follicle-stimulating-hormone receptor and twinning.
Gromoll J, Simoni M. Gromoll J, et al. Lancet. 2001 Jan 20;357(9251):230; author reply 231-2. doi: 10.1016/S0140-6736(05)71328-3. Lancet. 2001. PMID: 11213123 No abstract available.
Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome.
Conway GS, Conway E, Walker C, Hoppner W, Gromoll J, Simoni M. Conway GS, et al. Among authors: Gromoll J. Clin Endocrinol (Oxf). 1999 Jul;51(1):97-9. doi: 10.1046/j.1365-2265.1999.00745.x. Clin Endocrinol (Oxf). 1999. PMID: 10468971
Mutational analysis of the follicle-stimulating hormone (FSH) receptor in normal and infertile men: identification and characterization of two discrete FSH receptor isoforms.
Simoni M, Gromoll J, Höppner W, Kamischke A, Krafft T, Stähle D, Nieschlag E. Simoni M, et al. Among authors: Gromoll J. J Clin Endocrinol Metab. 1999 Feb;84(2):751-5. doi: 10.1210/jcem.84.2.5500. J Clin Endocrinol Metab. 1999. PMID: 10022448
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