Pille Tammur

Tartu, Estonia

Last Updated: 09/26/2026

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Found 14 publications

Macular and optic nerve hypoplasia in chromosome 2p partial trisomy.

Macular and optic nerve hypoplasia in chromosome 2p partial trisomy.

Journal: Ophthalmic genetics

Published: November 25, 2025

Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old With Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial.

Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old With Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial.

Journal: HemaSphere

Published: February 08, 2023

Telomere Architecture Correlates with Aggressiveness in Multiple Myeloma.

Telomere Architecture Correlates with Aggressiveness in Multiple Myeloma.

Journal: Cancers

Published: March 09, 2021

A two-year prospective study assessing the performance of fetal chromosomal microarray analysis and next-generation sequencing in high-risk pregnancies.

A two-year prospective study assessing the performance of fetal chromosomal microarray analysis and next-generation sequencing in high-risk pregnancies.

Journal: Molecular genetics & genomic medicine

Published: December 29, 2020

Distinct Nuclear Organization of Telomeresand Centromeres in Monoclonal Gammopathyof Undetermined Significance and Multiple Myeloma.

Distinct Nuclear Organization of Telomeresand Centromeres in Monoclonal Gammopathyof Undetermined Significance and Multiple Myeloma.

Journal: Cells

Published: June 18, 2019

Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency.

Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency.

Journal: Molecular genetics & genomic medicine

Published: June 07, 2019

Detection of a balanced translocation carrier through trophectoderm biopsy analysis: a case report.

Detection of a balanced translocation carrier through trophectoderm biopsy analysis: a case report.

Journal: Molecular cytogenetics

Published: February 09, 2019

The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental Consanguinity.

The Diagnostic Utility of Single Long Contiguous Stretches of Homozygosity in Patients without Parental Consanguinity.

Journal: Molecular syndromology

Published: June 30, 2015

Quantitative superresolution microscopy reveals differences in nuclear DNA organization of multiple myeloma and monoclonal gammopathy of undetermined significance.

Quantitative superresolution microscopy reveals differences in nuclear DNA organization of multiple myeloma and monoclonal gammopathy of undetermined significance.

Journal: Journal of cellular biochemistry

Published: December 02, 2014

De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis.

De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis.

Journal: European journal of medical genetics

Published: November 17, 2014

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience.

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience.

Journal: Molecular genetics & genomic medicine

Published: September 19, 2013

Three-dimensional Nuclear Telomere Organization in Multiple Myeloma.

Three-dimensional Nuclear Telomere Organization in Multiple Myeloma.

Journal: Translational oncology

Published: September 18, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026