Publications by authors named "Iris Bartels"

13Publications

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

Primate Biol 2019 29;6(2):75-86. Epub 2019 Jul 29.

Research Platform Degenerative Diseases, German Primate Center - Leibniz Institute for Primate Research, Kellnerweg 4, 37077 Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5194/pb-6-75-2019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041535PMC
July 2019

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

Mol Cytogenet 2018 29;11:62. Epub 2018 Dec 29.

1Institute of Human Genetics, University Medical Center, Heinrich-Düker-Weg 12, 37073 Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s13039-018-0410-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310980PMC
December 2018

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

Mol Cytogenet 2014 Jan 23;7(1). Epub 2014 Jan 23.

Institute of Human Genetics, Georg August University, Heinrich-Düker-Weg 12, 37073 Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1755-8166-7-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905920PMC
January 2014

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

Eur J Med Genet 2013 Aug 26;56(8):458-62. Epub 2013 Jun 26.

Institute of Human Genetics, University Medical Center Goettingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2013.06.002DOI Listing
August 2013

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

Eur J Med Genet 2012 Aug-Sep;55(8-9):480-4. Epub 2012 Jun 4.

Institute of Human Genetics, University of Göttingen, Heinrich-Düker-Weg 12, D-37073 Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2012.05.004DOI Listing
November 2012

Cell-free fetal DNA in specimen from pregnant women is stable up to 5 days.

Prenat Diagn 2011 Dec 26;31(13):1300-4. Epub 2011 Oct 26.

Department of Transfusion Medicine, University Medical Center, Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pd.2889DOI Listing
December 2011

The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible.

Transfusion 2008 Nov 7;48(11):2292-301. Epub 2008 Aug 7.

Department of Transfusion Medicine, Department of Human Genetics, University Medical Center, Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1537-2995.2008.01843.xDOI Listing
November 2008

Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay.

Am J Med Genet A 2007 May;143A(10):1091-9

Institut für Humangenetik, Georg-August-Universität Göttingen, Heinrich-Düker-Weg 12, Göttingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.31686DOI Listing
May 2007

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

Eur J Med Genet 2007 Mar-Apr;50(2):133-8. Epub 2006 Nov 10.

Institute of Human Genetics, University of Goettingen, Heinrich-Dueker-Weg 12, D-37073 Goettingen, Lower Saxonia, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2006.10.007DOI Listing
May 2007