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    • Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
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Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism. J Clin Invest. 2007 Feb; 117(2):457-63.

View in: PubMed

subject areas
  • Adult
  • Amino Acid Sequence
  • Base Sequence
  • Conserved Sequence
  • DNA
  • Female
  • Fibroblast Growth Factor 8
  • Genotype
  • Gonadotropin-Releasing Hormone
  • Heterozygote
  • Humans
  • Hypogonadism
  • Kallmann Syndrome
  • Male
  • Models, Genetic
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation
  • Pedigree
  • Phenotype
  • Receptor, Fibroblast Growth Factor, Type 1
  • Receptors, LHRH
  • Sequence Deletion
  • Sequence Homology, Amino Acid
  • Transcription Factors

authors with profiles
  • Shaun K. Olsen