Segregation of the marker chromosome der(20) in the sperm of a male with karyotype 46,XY/47,XY+mar[4].
Wiland E, Jarmuz M, Kurpisz M;
Med Sci Monit, 2005, 11 (3): CS9-15.
Publikacje
Publikacje pracowników w ePub
Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure.
Gajęcka M, Yu W, Ballif BC, Glotzbach D, Bailey KA, Shaw ChA, Kashork CD, Heilstedt HA, Ansel DA, Theisen A, Rice R, Rice DPC, Shaffer LG;
Eur J Hum Genet, 2005, 13 (2): 139-149.
Disruption of the BCL11B gene through inv(14)(Q11.2Q32.31) results in the expression of BCL11B-TRDC fusion transcripts and is associated with the absence of wild-type BCL11B transcripts in T-ALL.
Przybylski GK, Dik WA, Wanzeck J, Grabarczyk P, Majunke S, Martin-Subero JI, Siebert R, Dolken G, Ludwig WD, Verhaaf B, van Dongen JJM, Schmidt CA, Langerak AW;
Leukemia, 2005, 19: 210-218.
Hematopoietic chimerism after allogenic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridization.
Jółkowska J, Pieczonka A, Strabel T, Boruczkowski D, Wachowiak J, Bader P, Witt M;
BMC Blood Disorders, 2005, 5: 1-6.
Autologous skeletal myoblasts for myocardial regeneration.
Siminiak T, Kalmucki P, Kurpisz M;
J Interv Cardiol, 2004, 17 (6): 1-9.
Aparrent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss.
Krawczyński MR, Dmenska, H, Witt M;
J Appl Genet 2004; 45: 107-110.
PCD and RP: X-linked inheritance of both disorders.
Krawczyński MR, Witt M;
Pediatr Pulmonol, 2004 (1); 38: 88-89.
Chimeryzm komórkowy po transplantacji szpiku kostnego.
Jółkowska J, Witt M;
Acta Haematol Polon, 2004; 35: 321-328.
Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions.
Geremek M, Witt M;
J Appl Genet, 2004, 45: 347-362.
Mukowiscydoza rozpoznana u 36-letniego chorego.
Majka L, Witt M, Młynarczyk W, Nowicka A, Rutkiewicz E;
Pneumonol Alergol Pol, 2004; 72: 211-213.