Katalin Komlosi
Pecs, BA, Hungary
Last Updated: 09/26/2026
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Found 21 publications
Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine Homeostasis.
Journal: Current molecular medicine
Published: July 09, 2019
Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
Journal: BMC medical genetics
Published: December 11, 2017
Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations.
Journal: Pathology oncology research : POR
Published: March 29, 2017
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
Journal: BMC medical genetics
Published: December 13, 2016
Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene.
Journal: American journal of medical genetics. Part A
Published: February 17, 2016
Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype.
Journal: Molecular cytogenetics
Published: September 21, 2015
Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.
Journal: Molecular cytogenetics
Published: February 27, 2015
Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.
Journal: Molecular cytogenetics
Published: November 17, 2014
Identifying rare genomic disorders with array comparative genomic hybridization in Hungary
Journal: Orvosi hetilap
Published: February 26, 2014
Deletion of 4q28.3-31.23 in the background of multiple malformations with pulmonary hypertension.
Journal: Molecular cytogenetics
Published: January 24, 2014
Last Updated: 09/26/2026