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

This publication has 40 references indexed in Scilit:

• Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer
  Nature Genetics, 1994
• The 1993–94 Généthon human genetic linkage map
  Nature Genetics, 1994
• Molecular Cloning of the Testicular Follicle Stimulating Hormone Receptor of the Nonhuman Primate Macaca fascicularis and Identification of Multiple Transcripts in the Testis
  Biochemical and Biophysical Research Communications, 1993
• The Chromosomal Localization of the Human Follicle-Stimulating Hormone Receptor Gene (FSHR) on 2p21-p16 Is Similar to That of the Luteinizing Hormone Receptor Gene
  Genomics, 1993
• Molecular cloning of a truncated isoform of the human follicle stimulating hormone receptor
  Biochemical and Biophysical Research Communications, 1992
• Cloning and sequencing of human FSH receptor cDNA
  Biochemical and Biophysical Research Communications, 1991
• Cloning and sequencing of human LHhCG receptor cDNA
  Biochemical and Biophysical Research Communications, 1990
• Molecular cloning, sequence and functional expression of the cDNA for the human thyrotropin receptor
  Biochemical and Biophysical Research Communications, 1989
• Effects of gonadotrophin deficiency on follicular development in hypogonadal (hpg) mice
  Reproduction, 1986
• The Gonadotropin Resistant Ovary Syndrome
  Seminars in Reproductive Medicine, 1983