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Results: 1-5 |
Results: 5

Authors: Emberger, W Petek, E Kroisel, PM Zierler, H Wagner, K
Citation: W. Emberger et al., Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome, AM J MED G, 104(4), 2001, pp. 312-318

Authors: Emberger, W Petek, E Plecko-Startinig, B Kroisel, PM Zierler, H Wagner, K
Citation: W. Emberger et al., A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity, J MED GENET, 37(11), 2000, pp. 892-896

Authors: Holinski-Feder, E Reyniers, E Uhrig, S Golla, A Wauters, J Kroisel, P Bossuyt, P Rost, I Jedele, K Zierler, H Schwab, S Wildenauer, D Speicher, MR Willems, PJ Meitinger, T Kooy, RF
Citation: E. Holinski-feder et al., Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3), AM J HU GEN, 66(1), 2000, pp. 16-25

Authors: Plochl, E Vlasak, I Rittinger, O Bergendi, E Stopar, M Kurnik, P Nachtigall, M Zierler, H Rappold, GA Schiebel, K
Citation: E. Plochl et al., Clinical, cytogenetic and molecular analysis of three 46,XX males, J PED END M, 12(3), 1999, pp. 389-395

Authors: Petek, E Kroisel, PM Schuster, M Zierler, H Wagner, K
Citation: E. Petek et al., Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene, AM J MED G, 84(3), 1999, pp. 229-232
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