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Goidts, V., L. Armengol, W. Schempp, J. Conroy, N. Nowak, S. Muller, D. N. Cooper, X. Estivill, W. Enard, J. M. Szamalek, H. Hameister and H. Kehrer-Sawatzki: Identification of large-scale human-specific copy number differences by inter-species array comparative genomic hybridization. In: Human Genetics 119, 1-2, 185-198 (2006).
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Kehrer-Sawatzki, H., S. Tinschert and D. E. Jenne: Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region. In: Journal of Medical Genetics 40, 10, Seq. No.: e116 (2003).
Kehrer-Sawatzki, H., S. Tinschert and D. E. Jenne: Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region. In: Journal of Medical Genetics 40, 10, e116-e116 (2003).
Petek, E., D. E. Jenne, J. Smolle, B. Binder, W. Lasinger, C. Windpassinger, K. Wagner, P. M. Kroisel and H. Kehrer-Sawatzki: Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with only few manifestations. In: Journal of Medical Genetics 40, 7, 520-525 (2003).
Jenne, D. E., S. Tinschert, M. O. Dorschner, H. Hameister, K. Stephens and H. Kehrer-Sawatzki: Complete physical map and gene content of the human NFI tumor suppressor region in human and mouse. In: Genes Chromosomes & Cancer 37, 2, 111-120 (2003).
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