Camilla F. Skjelbred
Skien, Norway
Last Updated: 09/26/2026
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Found 8 publications
Hereditary peripheral neuropathies diagnosed by next-generation sequencing.
Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: November 05, 2015
Clinical exome sequencing – Norwegian findings.
Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: November 05, 2015
Variants in the genes DCTN2, DNAH10, LRIG3, and MYO1A are associated with intermediate Charcot-Marie-Tooth disease in a Norwegian family.
Journal: Acta neurologica Scandinavica
Published: September 11, 2015
Corrigendum to "Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing".
Journal: BioMed research international
Published: September 08, 2015
Copy number variations in a population-based study of Charcot-Marie-Tooth disease.
Journal: BioMed research international
Published: October 10, 2014
Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing.
Journal: BioMed research international
Published: February 27, 2014
Variant-beta luteinizing hormone is not associated with poor ovarian response to controlled ovarian hyperstimulation.
Journal: Reproductive biology and endocrinology : RB&E
Published: October 30, 2013
Increased risk of ovarian hyperstimulation syndrome following controlled ovarian hyperstimulation in patients with vascular endothelial growth factor +405 cc genotype.
Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
Published: May 17, 2012
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Last Updated: 09/26/2026