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Original Article

Hereditary hypergonadotropic primary amenorrhea

Pages 10-11 | Published online: 07 Jul 2009

References

  • Simpson J L, Christakos A C, Horwith M, Silverman F S. Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data. Birth Defects: Orig Article Series 1971; VII: 392–98
  • Aittomiki K. The genetics of XX gonadal dysgenesis. Am.J. Hum. Genet. 1994; 54: 844–51
  • Rousseau-Merck M. F., Atger M., Loosfelt H., Milgrom E., Berger R. The chromosomal localization of the human follicle-stimulating hormone receptor gene (FSHR) on 2p21-2p16 is similar to that of the luteinizing hormone receptor gene. Genomics 1993; 15: 222–24
  • Kelton C. A., Cheng S. V.Y., Nugent N. P., Schweickhardt R. L., Rosenthal J. L., Overton S. A., Wands G. D., Kuzeja J. B., Luchette C. A., Chappel S. C. The cloning of the human follicle stimulating hormone receptor and its expression in COS7, CHO, and Y-1 cells. Mol Cell Endocrinol. 1992; 89: 141–51
  • Aittomiki K, Dieguez Lucena J L, Pakarinen P, et al. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 1995; 82: 959–68

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