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Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, von Eggeling F, Liehr T. Starke H, et al. Among authors: seidel j. Hum Genet. 2003 Dec;114(1):51-67. doi: 10.1007/s00439-003-1016-3. Epub 2003 Sep 16. Hum Genet. 2003. PMID: 13680362
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.
Trifonov V, Seidel J, Starke H, Martina P, Beensen V, Ziegler M, Hartmann I, Heller A, Nietzel A, Claussen U, Liehr T. Trifonov V, et al. Among authors: seidel j. Prenat Diagn. 2003 May;23(5):427-30. doi: 10.1002/pd.595. Prenat Diagn. 2003. PMID: 12749042 No abstract available.
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: seidel j. Int J Mol Med. 2003 May;11(5):575-7. doi: 10.3892/ijmm.11.5.575. Int J Mol Med. 2003. PMID: 12684692
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
Seidel J, Heller A, Senger G, Starke H, Chudoba I, Kelbova C, Tönnies H, Neitzel H, Haase C, Beensen V, Zintl F, Claussen U, Liehr T. Seidel J, et al. Eur J Pediatr. 2003 Sep;162(9):582-8. doi: 10.1007/s00431-003-1254-3. Epub 2003 Jun 19. Eur J Pediatr. 2003. PMID: 12819962 Review.
629 results