Marianne Lodahl
Copenhagen, Denmark
Last Updated: 09/26/2026
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Found 10 publications
Meeting the demand: A collaborative approach in developing genetic counselling education in the Nordic countries.
Journal: Journal of community genetics
Published: December 17, 2025
Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.
Journal: European journal of human genetics : EJHG
Published: October 14, 2025
Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients.
Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients.
Journal: Scientific reports
Published: November 03, 2021
The Global State of the Genetic Counseling Profession.
Journal: European journal of human genetics : EJHG
Published: February 05, 2018
Phenotypic subregions within the split-hand/foot malformation 1 locus.
Journal: Human genetics
Published: August 31, 2015
Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation.
Journal: Gene
Published: October 14, 2014
Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal loss.
Journal: Mitochondrion
Published: March 11, 2013
SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations.
Journal: Clinical genetics
Published: September 17, 2012
GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in east Greenland.
Journal: International journal of audiology
Published: February 29, 2012
The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 05, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026