AAAAAA
Results:
1-7
|
Results: 7
Authors:
Dufke, A
Walczak, C
Liehr, T
Starke, H
Trifonov, V
Rubtsov, N
Schoning, M
Enders, H
Eggermann, T
Citation: A. Dufke et al., Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker, EUR J HUM G, 9(8), 2001, pp. 572-576
Authors:
Dufke, A
Mayrhofer, H
Enders, H
Kaiser, P
Leipoldt, M
Citation: A. Dufke et al., Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23), CYTOG C GEN, 93(3-4), 2001, pp. 168-170
Authors:
Binder, G
Eggermann, T
Enders, H
Ranke, MB
Dufke, A
Citation: G. Binder et al., Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome causedby a structurally altered X chromosome, J PEDIAT, 138(2), 2001, pp. 285-287
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:
Dufke, A
Eggermann, K
Balg, S
Stengel-Rutkowski, S
Enders, H
Kaiser, P
Citation: A. Dufke et al., A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p), CYTOG C GEN, 91(1-4), 2000, pp. 85-89
Authors:
Walczak, C
Enders, H
Grissinger, K
Dufke, A
Citation: C. Walczak et al., Retrospective diagnosis of trisomy 15 in formalin-fixed, paraffin-embeddedplacental tissue in a newborn girl with Prader-Willi syndrome, PRENAT DIAG, 20(11), 2000, pp. 914-916
Authors:
Eggermann, K
Dufke, A
Enders, H
Kaiser, P
Stotter, M
Eggerman, T
Citation: K. Eggermann et al., Rare case of de novo interstitial deletion 2q13q21: Clinical, cytogenetic,and molecular studies, AM J MED G, 92(2), 2000, pp. 153-154
Risultati:
1-7
|