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Evidence for a new microdeletion syndrome in 15q21.
Liehr T, Starke H, Heller A, Weise A, Beensen V, Senger G, Kittner G, Prechtel M, Claussen U, Seidel J. Liehr T, et al. Among authors: kittner g. Int J Mol Med. 2003 May;11(5):575-7. doi: 10.3892/ijmm.11.5.575. Int J Mol Med. 2003. PMID: 12684692
First case of trisomy 13 plus mosaic trisomy 1q.
Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U. Liehr T, et al. Among authors: kittner g. Fetal Diagn Ther. 2002 May-Jun;17(3):133-6. doi: 10.1159/000048025. Fetal Diagn Ther. 2002. PMID: 11914563