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                             24 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An isochromosome of the long arm of chromosome 18 in a patient with myelodysplastic syndrome with myelofibrosis Xue, Yongquan
1995
79 2 p. 149-152
4 p.
artikel
2 Are chromosome aberrations in circulating lymphocytes predictive of future cancer onset in humans? Preliminary results of an Italian cohort study Bonassi, Stefano
1995
79 2 p. 133-135
3 p.
artikel
3 Chromosomal changes in renal oncocytomas Evidence that t(5;11)(q35;q13) may characterize a second subgroup of oncocytomas van den Berg, E.
1995
79 2 p. 164-168
5 p.
artikel
4 Chromosomal instability in multiple endocrine neoplasia type 1 cytogenetic evaluation with DEB test Tomassetti, Paola
1995
79 2 p. 123-126
4 p.
artikel
5 Chromosome aberrations in desmoid tumors Trisomy 8 may be a predictor of recurrence Fletcher, Jonathan A.
1995
79 2 p. 139-143
5 p.
artikel
6 Chromosome abnormalities and p53 expression in a small cell carcinoma of the bladder Atkin, Niels B.
1995
79 2 p. 111-114
4 p.
artikel
7 Cytogenetic and FISH investigations on tetrasomy 8 in ANLL Starza, Roberta La
1995
79 2 p. 182-185
4 p.
artikel
8 Cytogenetic and flow cytometric analysis of a pancreatoblastoma Wiley, J.
1995
79 2 p. 115-118
4 p.
artikel
9 Cytogenetic changes in ovarian mucinous cystadenocarcinoma of low malignant potential with persistent pseudomyxoma peritonei Vasilev, Steven A.
1995
79 2 p. 160-163
4 p.
artikel
10 Deletion 6q in three cases of mixed type liposarcoma in addition to t(12;16)(q13;p11) Altungoz, Oguz
1995
79 2 p. 104-110
7 p.
artikel
11 Double-minute chromosomes appearing in a patient with myelodysplastic syndrome with disease evolution Ohyashiki, Kazuma
1995
79 2 p. 169-172
4 p.
artikel
12 Fluorescence in situ hybridization for the detection of trisomies 8 and 9 in polycythemia vera Amiel, A.
1995
79 2 p. 153-156
4 p.
artikel
13 Interphase cytogenetics of the t(8;21)(q22;q22) associated with acute myelogenous leukemia by two-color fluorescence in situ hybridization Sacchi, Nicoletta
1995
79 2 p. 97-103
7 p.
artikel
14 Involvement of chromosome 22 in ependymomas Wernicke, Catrin
1995
79 2 p. 173-176
4 p.
artikel
15 Is trisomy 4 a secondary chromosomal abnormality in acute myeloblastic leukemia? Bonomi, Rossana
1995
79 2 p. 186-187
2 p.
artikel
16 Monosomy 1p is correlated with enhanced in vivo glucose metabolism in meningiomas Henn, Wolfram
1995
79 2 p. 144-148
5 p.
artikel
17 Near-haploidy in two malignant fibrous histiocytomas Aspberg, Frida
1995
79 2 p. 119-122
4 p.
artikel
18 Supernumerary isochromosome 4p in ANLL-M4 myelomonocytic type is associated with favorable prognosis Hoo, Joe J.
1995
79 2 p. 127-129
3 p.
artikel
19 Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland Jin, Yuesheng
1995
79 2 p. 157-159
3 p.
artikel
20 Translocation (1;14)(p34;q11) and trisomy 8 in a T -cell acute lymphoblastic Leukemia patient Martín-Henao, Gregorio Angel
1995
79 2 p. 177-181
5 p.
artikel
21 Translocation (6;10)(p21;q22) in Uterine Leiomyomas Ozisik, Yavuz Y.
1995
79 2 p. 136-138
3 p.
artikel
22 Translocation (2;3)(p22;q28) is associated with myeloid disorders Berger, Roland
1995
79 2 p. 130-132
3 p.
artikel
23 Translocation(11;19)(q14–21;p12) in a parotid mucoepidermoid carcinoma of a child Dahlenfors, Rigmor
1995
79 2 p. 188-
1 p.
artikel
24 Trisomy 20 Characterizes a Second Group of Desmoid Tumors Dal Cin, P.
1995
79 2 p. 189-
1 p.
artikel
                             24 gevonden resultaten
 
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