Next generation phenotyping in Emanuel and Pallister‐Killian syndrome using computer‐aided facial dysmorphology analysis of 2D photos von Liehr, T., Acquarola, N., Pyle, K., St‐Pierre, S., Rinholm, M., Bar, O., Wilhelm, K., Schreyer, I.

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Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo von Aurich, H, Sgodda, M, Kaltwaßer, P, Vetter, M, Weise, A, Liehr, T, Brulport, M, Hengstler, J G, Dollinger, M M, Fleig, W E, Christ, B

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Complex chromosomal rearrangements: origin and meiotic behavior von Pellestor, F, Anahory, T, Lefort, G, Puechberty, J, Liehr, T, Hédon, B, Sarda, P

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Small supernumerary marker chromosomes (sSMC) in humans von Liehr, T., Claussen, U., Starke, H.

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Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae) von Yano, C F, Bertollo, L A C, Ezaz, T, Trifonov, V, Sember, A, Liehr, T, Cioffi, M B

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Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients von Ribeiro, I.P., Carreira, I.M., Esteves, L., Caramelo, F., Liehr, T., Melo, J.B.

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A New Case of Childhood Acute Lymphoblastic B-Cell Leukemia from Pristina von Graiqevci-Uka, V., Behluli, E., Spahiu, L., Liehr, T., Temaj, G.

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Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepa... von Winkler, S., Hempel, M., Brückner, S., Mallek, F., Weise, A., Liehr, T., Tautenhahn, H.-M., Bartels, M., Christ, B.

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7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder von Castiglia, L., Husain, R. A., Marquardt, I., Fink, C., Liehr, T., Serino, D., Elia, M., Coci, E. G.

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Comparative Chromosomal Mapping of Microsatellites in Leporinus Species (Characiformes, Anostomidae): Unequal Accumulation on the W Chromosomes von Poltronieri, J., Marquioni, V., Bertollo, L.A.C., Kejnovsky, E., Molina, W.F., Liehr, T., Cioffi, M.B.

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A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype von Papoulidis, I., Papageorgiou, E., Siomou, E., Oikonomidou, E., Thomaidis, L., Vetro, A., Zuffardi, O., Liehr, T., Manolakos, E., Vassilis, Papadopoulos

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A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) von Romero, V. I., Pozo, J. C., Saenz, S., Llamos-Paneque, A., Liehr, T., Hosomichi, K., Tajima, A.

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Independent Sex Chromosome Evolution in Lower Vertebrates: A Molecular Cytogenetic Overview in the Erythrinidae Fish Family von Cioffi, M.B., Liehr, T., Trifonov, V., Molina, W.F., Bertollo, L.A.C.

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Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic l... von Capela de Matos, RR, Othman, MAK, Ferreira, GM, Monteso, KCA, de Souza, MT, Rouxinol, M, Melo, JB, Carreira, IM, Abdelhay, E, Liehr, T, Ribeiro, RC, Silva, MLM

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Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes von Liehr, T., Klein, E., Mrasek, K., Kosyakova, N., Guilherme, R.S., Aust, N., Venner, C., Weise, A., Hamid, A.B.

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CYTOGENETIC AND CLINICAL DATA OF VARIANT THREE-WAY TRANSLOCATIONS T(8;V;21) IN CHILDHOOD ACUTE MYELOID LEUKEMIA von Matos, RRC, Monteso, KC, Bizarro, MT, Rocha, MM, Liehr, T, Rouxinol, M, Abdelhay, E, Binato, R, Ribeiro, RC

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QUANTITATIVE REAL-TIME PCR (RT-QPCR) COMPARING THE RELATIVE EXPRESSION LEVELS OF GENE TRANSCRIPTS INVOLVED IN A CRYPTIC THREE-WAY TRANSLOCATION T(9;11;19): AN ORIGINAL CASE OF AN I... von Ferreira, GM, Matos, RRC, Monteso, KC, Rocha, MM, Bizarro, MT, Meyer, C, Liehr, T, Abdelhay, E, Binato, R, Silva, MLM

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NTRK3 REARRANGEMENT IN A NON-ROBERTSONIAN T(15;21)(Q25.3;Q22.1) IN AN PEDIATRIC PATIENT WITH PROGENITOR B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA WITH THE IAMP21 von Matos, RRC, Ferreira, GM, Monteso, KC, Bizarro, MT, Othman, M, Liehr, T, Rouxinol, M, Abdelhay, E, Binato, R, Silva, MLM

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Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family von Supiwong, W, Liehr, T, Cioffi, M B, Chaveerach, A, Kosyakova, N, Fan, X, Tanee, T, Tanomtong, A

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Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation von Liehr, T., Mrasek, K., Weise, A., Dufke, A., Rodríguez, L., Martínez Guardia, N., Sanchís, A., Vermeesch, J.R., Ramel, C., Polityko, A., Haas, O.A., Anderson, J., Claussen, U., von Eggeling, F., Starke, H.

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