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Results:
1-9
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Results: 9
Authors:
Henrich, W
Schmider, A
Sarioglu, N
Neitzel, H
Citation: W. Henrich et al., Massive placental hemorrhage of partial hydatiforme mole due to complete autosomal triploidy (68,XX) - prenatal diagnosis and clinical sequelae, Z GEBU NEON, 205(3), 2001, pp. 114-116
Authors:
Musebeck, J
Mohnike, K
Beye, P
Tonnies, H
Neitzel, H
Schnabel, D
Gruters, A
Wieacker, PF
Stumm, M
Citation: J. Musebeck et al., Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature, EUR J PED, 160(9), 2001, pp. 561-565
Authors:
Tonnies, H
Stumm, M
Wegner, RD
Chudoba, I
Kalscheuer, V
Neitzel, H
Citation: H. Tonnies et al., Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics, CYTOG C GEN, 93(3-4), 2001, pp. 188-194
Authors:
Tonnies, H
Schulze, I
Hennies, HC
Neumann, LM
Keitzer, R
Neitzel, H
Citation: H. Tonnies et al., De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes, J MED GENET, 38(9), 2001, pp. 617-621
Authors:
Tonnies, H
Toliat, MR
Ramel, C
Pape, UF
Neitzel, H
Berger, W
Wiedenmann, B
Citation: H. Tonnies et al., Analysis of sporadic neuroendocrine rumours of the enteropancreatic systemby comparative genomic hybridisation, GUT, 48(4), 2001, pp. 536-541
Authors:
Melcher, R
von Golitschek, R
Steinlein, C
Schindler, D
Neitzel, H
Kainer, K
Schmid, M
Hoehn, H
Citation: R. Melcher et al., Spectral karyotyping of Werner syndrome fibroblast cultures, CYTOG C GEN, 91(1-4), 2000, pp. 180-185
Authors:
Singh, AP
Henschel, S
Sperling, K
Kalscheuer, V
Neitzel, H
Citation: Ap. Singh et al., Differences in the meiotic pairing behavior of gonosomal heterochromatin between female and male Microtus agrestis: implications for the mechanism ofheterochromatin amplification on the X and Y, CYTOG C GEN, 91(1-4), 2000, pp. 253-260
Authors:
Weimer, J
Kiechle, M
Wiedemann, U
Tonnies, H
Neitzel, H
Ruhenstroth, E
Ovens-Raeder, A
Arnold, N
Citation: J. Weimer et al., Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot, J MED GENET, 37(6), 2000, pp. 442-445
Authors:
Zouboulis, CC
Seltmann, H
Neitzel, H
Orfanos, CE
Citation: Cc. Zouboulis et al., Establishment and characterization of an immortalized human sebaceous gland cell line (SZ95), J INVES DER, 113(6), 1999, pp. 1011-1020
Risultati:
1-9
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