Author Bartels, Iris
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2007 | Journal Article
An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype
Bartels, I.; Starke, H.; Argyriou, L.; Sauter, S. M.; Zoll, B. & Liehr, T. (2007)
European Journal of Medical Genetics, 50(2) pp. 133-138. DOI: https://doi.org/10.1016/j.ejmg.2006.10.007
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2007 | Journal Article
Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay
Sauter, S. M.; Boehm, D.; Bartels, I.; Burfeind, P.; Laccone, F. A.; Neesen, J. & Wilken, B. et al. (2007)
American Journal of Medical Genetics Part A, 143A(10) pp. 1091-1099. DOI: https://doi.org/10.1002/ajmg.a.31686
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2008 | Journal Article |
The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible
Mueller, S. P.; Bartels, I.; Stein, W.; Emons, G.; Gutensohn, K.; Koehler, M. & Legler, T. J. (2008)
Transfusion, 48(11) pp. 2292-2301. DOI: https://doi.org/10.1111/j.1537-2995.2008.01843.x
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2009 | Journal Article |
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation
Auber, B.; Bruemmer, V.; Zoll, B.; Burfeind, P.; Boehm, D.; Liehr, T. & Brockmann, K. et al. (2009)
Molecular Cytogenetics, 2 art. 10. DOI: https://doi.org/10.1186/1755-8166-2-10
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2011 | Journal Article
Cell-free fetal DNA in specimen from pregnant women is stable up to 5?days
Mueller, S. P.; Bartels, I.; Stein, W.; Emons, G.; Gutensohn, K. & Legler, T. J. (2011)
Prenatal Diagnosis, 31(13) pp. 1300-1304. DOI: https://doi.org/10.1002/pd.2889
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2012 | Journal Article
A 16q12 Microdeletion in a Boy With Severe Psychomotor Delay, Craniofacial Dysmorphism, Brain and Limb Malformations, and a Heart Defect
Shoukier, M.; Wickert, J.; Schroeder, J.; Bartels, I.; Auber, B.; Zoll, B. & Salinas-Riester, G. et al. (2012)
American Journal of Medical Genetics Part A, 158A(1) pp. 229-235. DOI: https://doi.org/10.1002/ajmg.a.34387
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2012 | Journal Article
Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
Pauli, S.; Schmidt, T.; Funke, R.; Zoll, B.; Burfeind, P.; Dybowski, U. & Shoukier, M. et al. (2012)
European Journal of Medical Genetics, 55(8-9) pp. 480-484. DOI: https://doi.org/10.1016/j.ejmg.2012.05.004
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2013 | Journal Article
Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p
Bartels, I.; Puetz, I.; Reintjes, N.; Netzer, C. & Shoukier, M. (2013)
European Journal of Medical Genetics, 56(8) pp. 458-462. DOI: https://doi.org/10.1016/j.ejmg.2013.06.002
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2014 | Journal Article |
De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis
Schwaibold, E. M. C.; Bartels, I.; Kuester, H.; Lorenz, M.; Burfeind, P.; Adam, R. & Zoll, B. (2014)
Molecular Cytogenetics, 7 art. 7. DOI: https://doi.org/10.1186/1755-8166-7-7
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2018 | Journal Article |
Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22
Schnabel, F.; Smogavec, M.; Funke, R.; Pauli, S.; Burfeind, P. & Bartels, I. (2018)
Molecular Cytogenetics, 11(1) art. 62. DOI: https://doi.org/10.1186/s13039-018-0410-4
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2019 | Journal Article
Baboon induced pluripotent stem cell generation by piggyBac transposition of reprogramming factors
Rodriguez-Polo, I.; Stauske, M.; Becker, A.; Bartels, I.; Dressel, R. & Behr, R. (2019)
Primate Biology, 6(2) pp. 75-86. DOI: https://doi.org/10.5194/pb-6-75-2019
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2020 | Journal Article |
Non-Human Primate iPSC Generation, Cultivation, and Cardiac Differentiation under Chemically Defined Conditions
Stauske, M.; Rodriguez Polo, I.; Haas, W.; Knorr, D. Y.; Borchert, T. ; Streckfuss-Bömeke, K. & Dressel, R. et al. (2020)
Cells, 9(6) pp. 1349. DOI: https://doi.org/10.3390/cells9061349
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