Merve Guvenc-Saka
Izmir, Turkey
Last Updated: 09/26/2026
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Found 10 publications
Characterization of the molecular and clinical features of Multilocus Inherited Neoplasia Allelic Syndrome (MINAS) cases in the Turkish population.
Journal: Familial cancer
Published: March 11, 2026
Duplication in the SHOX Gene as a Rare Genetic Cause of Short Stature and/or Skeletal Abnormalities: A Clinical Report and Review of the Literature.
Journal: Journal of clinical research in pediatric endocrinology
Published: July 09, 2025
Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: June 24, 2025
The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis.
Journal: The clinical respiratory journal
Published: April 07, 2020
Clinical and exome sequencing findings in seven children with Bardet-Biedl syndrome from Turkey.
Journal: Annals of human genetics
Published: February 11, 2020
Could high levels of cell-free DNA in maternal blood be associated with maternal health and perinatal outcomes?
Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: November 27, 2019
A new mutation associated with Pierson syndrome.
Journal: Archivos argentinos de pediatria
Published: March 25, 2019
Targeted fetal cell-free DNA screening for aneuploidies in 4,594 pregnancies: Single center study.
Journal: Molecular genetics & genomic medicine
Published: December 18, 2018
Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes.
Journal: International journal of immunogenetics
Published: December 08, 2018
Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability.
Journal: Journal of pediatric genetics
Published: October 07, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026