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.
Publikacje
Publikacje pracowników w ePub
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.
The sequence variant of NOD2/CARD 15 in a Polish family on the background of Polish patients with Crohn's disease.
Dobrowolska-Zachwieja A, Kaczmarek M, Hoppe-Gołębiewska J, Słomski R;
Gastroenterolo Pol, 2004, 11 (4): 325-331.
The influence of the NOD2/CARD15 gene mutation variant on the incidence of extrainstestinal symptoms in patients with Crohn's disease in a Polish population.
Dobrowolska-Zachwieja A, Kaczmarek M, Hoppe-Gołębiewska J, Kalak R, Słomski R, Linke K;
Now Lek, 2004, 73 (5): 337-348.
The normotensive carriers of the MTHFR 677T allele, displaying the increased risk of development of the abdominal aortic aneurysm (AAA), occur at the highest frequency among the smoking patients.
Strauss E, Waliszewski K, Pawlak AL;
Prz Lek. 2004; 61 (10): 1086-1089.
Controversial aspect of using GFP as a marker for the production of transgenic cattle.
Duszewska AM, Lipiński D, Piliszek A, Słomski R, Pławski A, Wojdan J, Gawron W, Juzwa W, Zeyland J, Wenta-Muchalska E, Reklewski Z;
Pol J Vet Sci, 2004, 7 (4): 24124-9.
Assessment of transgene inheritance and transgene mapping in rabbits producing the human growth hormone in milk.
Kalak R, Lipiński D, Wielgus K, Jarmuż M, Jura J, Szalata M, Michalak M, Pławski A, Kaczmarek M, Nuc K, Korcz A, Gronek P, Smorąg Z, Pienkowski M, Słomski R;
Ann Anim Sc, 2004, 4; 241-252.