Iris Bartels

Robert Koch Str. 40
Goettingen, NI 37075, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation.

A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation.

Journal: Scientific reports

Published: December 01, 2020

Non-Human Primate iPSC Generation, Cultivation, and Cardiac Differentiation under Chemically Defined Conditions.

Non-Human Primate iPSC Generation, Cultivation, and Cardiac Differentiation under Chemically Defined Conditions.

Journal: Cells

Published: April 28, 2020

Baboon induced pluripotent stem cell generation by piggyBac transposition of reprogramming factors.

Baboon induced pluripotent stem cell generation by piggyBac transposition of reprogramming factors.

Journal: Primate biology

Published: April 11, 2019

Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22.

Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22.

Journal: Molecular cytogenetics

Published: July 26, 2018

De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis.

De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis.

Journal: Molecular cytogenetics

Published: November 16, 2013

Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8.

Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8.

Journal: Cytogenetic and genome research

Published: July 23, 2013

Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p.

Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p.

Journal: European journal of medical genetics

Published: February 07, 2013

A family with an inverted tandem duplication 5q22.1q23.2.

A family with an inverted tandem duplication 5q22.1q23.2.

Journal: Cytogenetic and genome research

Published: July 16, 2012

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?

Journal: Clinical genetics

Published: January 31, 2012

Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes.

Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes.

Journal: European journal of medical genetics

Published: October 09, 2011

Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.

Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.

Journal: Molecular cytogenetics

Published: January 19, 2009

An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.

An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.

Journal: European journal of medical genetics

Published: August 24, 2006

Showing 1-12 of 13

Last Updated: 09/26/2026