Preoperative joint line convergence angle correction is a key factor in optimising accuracy in varus knee correction osteotomy
Behrendt, P., Akoto, R., Bartels, I., Thürig, G., Fahlbusch, H., Korthaus, A., Dalos, D., Hoffmann, M., Frosch, K.-H., Krause, M.
Published in Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA (01.04.2023)
Published in Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA (01.04.2023)
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Journal Article
Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
Shoukier, M, Klein, N, Auber, B, Wickert, J, Schröder, J, Zoll, B, Burfeind, P, Bartels, I, Alsat, EA, Lingen, M, Grzmil, P, Schulze, S, Keyser, J, Weise, D, Borchers, M, Hobbiebrunken, E, Röbl, M, Gärtner, J, Brockmann, K, Zirn, B
Published in Clinical genetics (01.01.2013)
Published in Clinical genetics (01.01.2013)
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Journal Article
A Family with an Inverted Tandem Duplication 5q22.1q23.2
Schmidt, T., Bartels, I., Liehr, T., Burfeind, P., Zoll, B., Shoukier, M.
Published in Cytogenetic and genome research (01.01.2013)
Published in Cytogenetic and genome research (01.01.2013)
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Journal Article
Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8
Schmidt, T., Bierhals, T., Kortüm, F., Bartels, I., Liehr, T., Burfeind, P., Shoukier, M., Frank, V., Bergmann, C., Kutsche, K.
Published in Cytogenetic and genome research (01.01.2014)
Published in Cytogenetic and genome research (01.01.2014)
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Journal Article
An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patient
Auber, B, Burfeind, P, Thiels, C, Alsat, EA, Shoukier, M, Liehr, T, Nelle, H, Bartels, I, Salinas-Riester, G, Laccone, F
Published in Clinical genetics (01.06.2010)
Published in Clinical genetics (01.06.2010)
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Journal Article
Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?
Liehr, T., Bartels, I., Zoll, B., Ewers, E., Mrasek, K., Kosyakova, N., Merkas, M., Hamid, A.B., von Eggeling, F., Posorski, N., Weise, A.
Published in Cytogenetic and genome research (01.01.2011)
Published in Cytogenetic and genome research (01.01.2011)
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Journal Article
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints
Manvelyan, M, Schreyer, I, Höls-Herpertz, I, Köhler, S, Niemann, R, Hehr, U, Belitz, B, Bartels, I, Götz, J, Huhle, D, Kossakiewicz, M, Tittelbach, H, Neubauer, S, Polityko, A, Mazauric, M.-L, Wegner, R, Stumm, M, Küpferling, P, Süss, F, Kunze, H, Weise, A, Liehr, T, Mrasek, K
Published in International journal of molecular medicine (01.06.2007)
Published in International journal of molecular medicine (01.06.2007)
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Journal Article
Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q
Bœhm, D., Laccone, F., Burfeind, P., Herold, S., Schubert, C., Zoll, B., Männer, J., Pauer, H. U., Bartels, I.
Published in Prenatal diagnosis (01.03.2006)
Published in Prenatal diagnosis (01.03.2006)
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Journal Article
Small Supernumerary Marker Chromosomes (sSMC) in Patients with a 45,X/46,X,+mar Karyotype – 17 New Cases and a Review of the Literature
Liehr, T., Mrasek, K., Hinreiner, S., Reich, D., Ewers, E., Bartels, I., Seidel, J., Emmanuil, N., Petesen, M., Polityko, A., Dufke, A., Iourov, I., Trifonov, V., Vermeesch, J., Weise, A.
Published in Sexual development (01.01.2007)
Published in Sexual development (01.01.2007)
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Journal Article
Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome
Meins, M, Burfeind, P, Motsch, S, Trappe, R, Bartmus, D, Langer, S, Speicher, M R, Mühlendyck, H, Bartels, I, Zoll, B
Published in Journal of medical genetics (01.05.2003)
Published in Journal of medical genetics (01.05.2003)
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Journal Article
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chromosome formation
Bartels, I., Schlueter, G., Liehr, T., von Eggeling, F., Starke, H., Glaubitz, R., Burfeind, P.
Published in Cytogenetic and genome research (01.01.2003)
Published in Cytogenetic and genome research (01.01.2003)
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Journal Article
Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion
Böhm, D., Hoffmann, K., Laccone, F., Wilken, B., Dechent, P., Frahm, J., Bartels, I., Bohlander, S.K.
Published in American journal of medical genetics. Part A (15.02.2006)
Published in American journal of medical genetics. Part A (15.02.2006)
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Journal Article
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay
von Beust, G., Sauter, S.M., Liehr, T., Burfeind, P., Bartels, I., Starke, H., von Eggeling, F., Zoll, B.
Published in American journal of medical genetics. Part A (15.08.2005)
Published in American journal of medical genetics. Part A (15.08.2005)
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Journal Article
Pseudo dicentric chromosome (5;21) : a rare example of maternal germline mosaicism
ENGEL, U, BOHLANDER, S. K, BINK, K, HINNEY, B, LACCONE, F, BARTELS, I
Published in Human reproduction (Oxford) (2001)
Published in Human reproduction (Oxford) (2001)
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Journal Article
First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome
Meins, M., Böhm, D., Großmann, A., Herting, E., Fleckenstein, B., Fauth, C., Speicher, M.R., Schindler, R., Zoll, B., Bartels, I., Burfeind, Peter
Published in American journal of medical genetics. Part A (15.05.2004)
Published in American journal of medical genetics. Part A (15.05.2004)
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Journal Article
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis
Trappe, R., Böhm, D., Kohlhase, J., Weise, A., Liehr, T., Essers, G., Meins, M., Zoll, B., Bartels, I., Burfeind, P.
Published in Cytogenetic and genome research (01.01.2002)
Published in Cytogenetic and genome research (01.01.2002)
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Journal Article