Cytogenetic contribution to uniparental disomy (UPD)

por Liehr, Thomas
Publicado 2010

Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes

por Liehr, Thomas
Publicado 2014

Small supernumerary marker chromosomes – an update

por Liehr, Thomas
Publicado 2014

Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants

por Liehr, Thomas
Publicado 2016

“Classical cytogenetics” is not equal to “banding cytogenetics”

por Liehr, Thomas
Publicado 2017

From Human Cytogenetics to Human Chromosomics

por Liehr, Thomas
Publicado 2019

Repetitive Elements in Humans

por Liehr, Thomas
Publicado 2021

About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ens...

por Liehr, Thomas
Publicado 2021

Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?

por Liehr, Thomas
Publicado 2021

Molecular Cytogenetics in the Era of Chromosomics and Cytogenomic Approaches

por Liehr, Thomas
Publicado 2021

Uniparental disomy is a chromosomic disorder in the first place

por Liehr, Thomas
Publicado 2022

False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests?

por Liehr, Thomas
Publicado 2022

Chromosomal Heteromorphisms and Cancer Susceptibility Revisited

por Liehr, Thomas
Publicado 2022

Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review

por Liehr, Thomas, Al-Rikabi, Ahmed
Publicado 2019

Reviewer acknowledgement 2013

por Liehr, Thomas, Heng, Henry, Yurov, Yuri
Publicado 2013

Reviewer acknowledgement 2014

por Liehr, Thomas, Heng, Henry, Yurov, Yuri
Publicado 2014

Cytogenomic characteristics of murine breast cancer cell line JC

por Azawi, Shaymaa, Rincic, Martina, Liehr, Thomas
Publicado 2021

A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case

por AL-ACHKAR, WALID, WAFA, ABDULSAMAD, LIEHR, THOMAS
Publicado 2013

Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting

por Rinčić, Martina, Iourov, Ivan Y., Liehr, Thomas
Publicado 2016

Next‐generation phenotyping in cat‐eye syndrome based on computer‐aided facial dysmorphology analysis of normal photographs

por Liehr, Thomas, Fleischer, Nicole, Al‐Rikabi, Ahmed
Publicado 2021