Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2

Anna-Pauliina Iivonen, Juho Kärkinen, Venkatram Yellapragada, Virpi Sidoroff, Henrikki Almusa, Kirsi Vaaralahti, Taneli Raivio

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalEuropean Journal of Endocrinology
Volume185
Issue number1
Pages (from-to)57-66
Number of pages10
ISSN0804-4643
DOIs
Publication statusPublished - Jan 2021
MoE publication typeA1 Journal article-refereed

Fields of Science

  • 3121 General medicine, internal medicine and other clinical medicine
  • GENOME-WIDE ASSOCIATION
  • HYPOGONADOTROPIC HYPOGONADISM
  • MESSENGER-RNA
  • BETA-CATENIN
  • EXPRESSION
  • GENE
  • PREDICTION
  • FEATURES
  • PUBERTY
  • LOCI

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