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Updated: May 31, 2026

Mutagenesis and Analysis of Genetic Mutations in the GC-rich KISS1 Receptor Sequence Identified in Humans with Reproductive Disorders
12:49

Mutagenesis and Analysis of Genetic Mutations in the GC-rich KISS1 Receptor Sequence Identified in Humans with Reproductive Disorders

Published on: September 4, 2011

Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland

Eeva-Maria Laitinen1, Kirsi Vaaralahti, Johanna Tommiska

  • 1Children's Hospital, Helsinki University Central Hospital, University of Helsinki, FI-00029 Helsinki, Finland.

Orphanet Journal of Rare Diseases
|June 21, 2011
PubMed
Abstract

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