AAAAAA
Results:
1-12
|
Results: 12
Authors:
Kinne, RW
Liehr, T
Beensen, V
Kunisch, E
Zimmermann, T
Holland, H
Pfeiffer, R
Stahl, HD
Lungershausen, W
Hein, G
Roth, A
Emmrich, F
Claussen, U
Froster, UG
Citation: Rw. Kinne et al., Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases, ARTHRITIS R, 3(5), 2001, pp. 319-330
Authors:
Frober, R
Kohoutek, T
Kahler, C
Beensen, V
Hauschild, R
Schulze, E
Linss, W
Citation: R. Frober et al., Pulmonary atresia with hypoplastic right ventricle - A clinical embryological study, FETAL DIAGN, 16(5), 2001, pp. 274-279
Authors:
Nietzel, A
Rocchi, M
Starke, H
Heller, A
Fiedler, W
Wlodarska, I
Loncarevic, IF
Beensen, V
Claussen, U
Liehr, T
Citation: A. Nietzel et al., A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH), HUM GENET, 108(3), 2001, pp. 199-204
Authors:
Liehr, T
Beensen, V
Hauschild, R
Ziegler, M
Hartmann, I
Starke, H
Heller, A
Kahler, C
Schmidt, M
Reiber, W
Hesse, M
Claussen, U
Citation: T. Liehr et al., Pitfalls of rapid prenatal diagnosis using the interphase nucleus, PRENAT DIAG, 21(5), 2001, pp. 419-421
Authors:
Liehr, T
Beensen, V
Starke, H
Hauschild, R
Hempell, E
Fritsche, V
Hoppe, C
Grosswendt, G
Prechtel, M
Ziegler, M
Claussen, U
von Eggeling, F
Citation: T. Liehr et al., Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21, CLIN GENET, 60(1), 2001, pp. 83-85
Authors:
Seidel, J
Schiller, S
Kelbova, C
Beensen, V
Orth, U
Vogt, S
Claussen, U
Zintl, F
Rappold, GA
Citation: J. Seidel et al., Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation, CLIN GENET, 59(2), 2001, pp. 115-121
Authors:
Hubler, A
Seidel, J
Kauf, E
Schramm, D
Beensen, V
Heller, A
Liehr, T
Zintl, F
Citation: A. Hubler et al., Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12(th) week of life, J PED END M, 13(4), 2000, pp. 445-450
Authors:
Dufke, A
Seidel, J
Schoning, M
Dobler-Neumann, M
Kelbova, C
Liehr, T
Beensen, V
Backsch, C
Klein-Vogler, U
Enders, H
Citation: A. Dufke et al., Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome, CYTOG C GEN, 91(1-4), 2000, pp. 81-84
Authors:
Heller, A
Seidel, J
Hubler, A
Starke, H
Beensen, V
Senger, G
Rocchi, M
Wirth, J
Chudoba, I
Claussen, U
Liehr, T
Citation: A. Heller et al., Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review, J MED GENET, 37(7), 2000, pp. 529-532
Authors:
Liehr, T
Starke, H
Beensen, V
Kahler, C
Harbich, M
Brude, E
Ziegler, M
Claussen, U
Citation: T. Liehr et al., Translocation trisomy dup(21q) and free trisomy 21 can be distinguished byinterphase-FISH, INT J MOL M, 3(1), 1999, pp. 11-14
Authors:
Chudoba, I
Franke, Y
Senger, G
Sauerbrei, G
Demuth, S
Beensen, V
Neumann, A
Hansmann, I
Claussen, U
Citation: I. Chudoba et al., Maternal UPD 20 in a hyperactive child with severe growth retardation, EUR J HUM G, 7(5), 1999, pp. 533-540
Authors:
Starke, H
Schreyer, I
Kahler, C
Fiedler, W
Beensen, V
Heller, A
Nietzel, A
Claussen, U
Liehr, T
Citation: H. Starke et al., Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8, PRENAT DIAG, 19(12), 1999, pp. 1169-1174
Risultati:
1-12
|