Genetic background of HSH in three Polish families and a patient with an X;9 translocation

R Jalkanen, E Pronicka, H Tyynismaa, A Hanauer, R Walder, T Alitalo

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume14
Pages (from-to)55-62
Number of pages8
ISSN1018-4813
DOIs
Publication statusPublished - 2006
MoE publication typeA1 Journal article-refereed

Fields of Science

  • hypomagnesemia
  • secondary hypocalcemia
  • TRPM6
  • mutation analysis
  • translocation breakpoint
  • ENDOTHELIAL GROWTH-FACTOR
  • SECONDARY HYPOCALCEMIA
  • VEGF-D
  • X-CHROMOSOME
  • HYPOMAGNESEMIA
  • CHANNEL
  • MUTATIONS
  • PCR
  • DNA

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