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

Cite this

@article{fffa71bb4dff475a8a29927693f10319,
title = "Genetic background of HSH in three Polish families and a patient with an X;9 translocation",
keywords = "hypomagnesemia, secondary hypocalcemia, TRPM6, mutation analysis, translocation breakpoint, ENDOTHELIAL GROWTH-FACTOR, SECONDARY HYPOCALCEMIA, VEGF-D, X-CHROMOSOME, HYPOMAGNESEMIA, CHANNEL, MUTATIONS, PCR, DNA",
author = "R Jalkanen and E Pronicka and H Tyynismaa and A Hanauer and R Walder and T Alitalo",
year = "2006",
doi = "10.1038/sj.ejhg.5201515",
language = "English",
volume = "14",
pages = "55--62",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",

}

Genetic background of HSH in three Polish families and a patient with an X;9 translocation. / Jalkanen, R ; Pronicka, E ; Tyynismaa, H ; Hanauer, A ; Walder, R ; Alitalo, T .

In: European Journal of Human Genetics, Vol. 14, 2006, p. 55-62.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - Genetic background of HSH in three Polish families and a patient with an X;9 translocation

AU - Jalkanen, R

AU - Pronicka, E

AU - Tyynismaa, H

AU - Hanauer, A

AU - Walder, R

AU - Alitalo, T

PY - 2006

Y1 - 2006

KW - hypomagnesemia

KW - secondary hypocalcemia

KW - TRPM6

KW - mutation analysis

KW - translocation breakpoint

KW - ENDOTHELIAL GROWTH-FACTOR

KW - SECONDARY HYPOCALCEMIA

KW - VEGF-D

KW - X-CHROMOSOME

KW - HYPOMAGNESEMIA

KW - CHANNEL

KW - MUTATIONS

KW - PCR

KW - DNA

U2 - 10.1038/sj.ejhg.5201515

DO - 10.1038/sj.ejhg.5201515

M3 - Article

VL - 14

SP - 55

EP - 62

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

ER -