| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia
|
Beverstock, Geoffrey C.
|
|
1996
|
89 |
2 |
p. 132-135
4 p.
|
artikel
|
| 2 |
Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberans
|
Pedeutour, F.
|
|
1996
|
89 |
2 |
p. 175-176
2 p.
|
artikel
|
| 3 |
A Philadelphia chromosome positive CML patient with a unique translocation studied via GTG-banding and fluorescence in situ hybridization
|
Young, Carolyn
|
|
1996
|
89 |
2 |
p. 157-162
6 p.
|
artikel
|
| 4 |
A subtle deletion of 12p by routine cytogenetics is found to be a translocation to 21q by fluorescence in situ hybridization: t(12;21)(p13;q22)
|
Filatov, Leonid V.
|
|
1996
|
89 |
2 |
p. 136-140
5 p.
|
artikel
|
| 5 |
Comparative genomic hybridization of germ cell tumors of the adult testis: Confirmation of karyotypic findings and identification of a 12p-amplicon
|
Mostert, M.M.C.
|
|
1996
|
89 |
2 |
p. 146-152
7 p.
|
artikel
|
| 6 |
Detection of aneuploidy in interphase nuclei from non-small cell lung carcinomas by fluorescence in situ hybridization using chromosome-specific repetitive DNA probes
|
Taguchi, Takahiro
|
|
1996
|
89 |
2 |
p. 120-125
6 p.
|
artikel
|
| 7 |
Detection of chromosomal abnormalities in uterine leiomyoma using conventional cytogenetic method and interphase fluorescence in situ hybridization
|
Hayashi, Satoshi
|
|
1996
|
89 |
2 |
p. 98-104
7 p.
|
artikel
|
| 8 |
Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridization
|
Tosi, Sabrina
|
|
1996
|
89 |
2 |
p. 153-156
4 p.
|
artikel
|
| 9 |
Duplication of chromosome 9 carrying a BCR/ABL chimeric gene in Philadelphia chromosome negative chronic myeloid leukemia
|
Takahashi, Naoto
|
|
1996
|
89 |
2 |
p. 166-169
4 p.
|
artikel
|
| 10 |
Evidence for somatic pairing of chromosome 7 and 10 homologs in a follicular lymphoma
|
Atkin, Niels B.
|
|
1996
|
89 |
2 |
p. 129-131
3 p.
|
artikel
|
| 11 |
Familial supernumerary chromosome and malignancy
|
Milunsky, Jeffrey M.
|
|
1996
|
89 |
2 |
p. 170-172
3 p.
|
artikel
|
| 12 |
ider(9)(q10)t(9;22)(q34;q11) is a recurrent chromosomal abnormality in acute lymphoblastic leukemia and lymphatic blastic phase of chronic myelogenous leukemia
|
Dierlamm, Judith
|
|
1996
|
89 |
2 |
p. 109-113
5 p.
|
artikel
|
| 13 |
Monosomy 22 in two ovarian granulosa cell tumors
|
Lindgren, Valerie
|
|
1996
|
89 |
2 |
p. 93-97
5 p.
|
artikel
|
| 14 |
Monozygotic twins with congenital acute lymphoblastic leukemia (ALL) and t(4;11)(q21;q23)
|
Bayar, Emel
|
|
1996
|
89 |
2 |
p. 177-180
4 p.
|
artikel
|
| 15 |
No evidence for the amplifications of MDM2 and C-myc genes involved in the genetic susceptibility to esophageal cancer in a high-risk area of North China
|
Zhu, Dan
|
|
1996
|
89 |
2 |
p. 184-185
2 p.
|
artikel
|
| 16 |
Partial deletion of the long arm of chromosome 5: A fluorescence in situ hybridization study using band-specific painting probes generated by chromosome microdissection
|
Tigaud, Isabelle
|
|
1996
|
89 |
2 |
p. 126-128
3 p.
|
artikel
|
| 17 |
Restriction endonuclease in situ digestion (REISD) and fluorescence in situ hybridization (FISH) as complementary methods to analyze chimerism and residual disease after bone marrow transplantation
|
Gosálvez, J.
|
|
1996
|
89 |
2 |
p. 141-145
5 p.
|
artikel
|
| 18 |
Significance of lymphocytic sister chromatid exchange frequencies in ovarian cancer patients
|
Dhar, Pawan Kumar
|
|
1996
|
89 |
2 |
p. 105-108
4 p.
|
artikel
|
| 19 |
Thymoma with a t(15;22)(p11;q11)
|
Dal Cin, Paola
|
|
1996
|
89 |
2 |
p. 181-183
3 p.
|
artikel
|
| 20 |
t(12;20)(q13;p11.2)—A new translocation involving the 12q13 breakpoint in acute nonlymphoblastic leukemia
|
Raanani, Pia
|
|
1996
|
89 |
2 |
p. 118-119
2 p.
|
artikel
|
| 21 |
t(5;12)(q31;q24) in childhood acute lymphoblastic leukemia
|
Tusell, Laura
|
|
1996
|
89 |
2 |
p. 163-165
3 p.
|
artikel
|
| 22 |
Trisomy 10: Age and leukemic lineage associations
|
Morgan, Rodman
|
|
1996
|
89 |
2 |
p. 173-174
2 p.
|
artikel
|
| 23 |
Trisomy 10 in acute myeloid leukemia
|
Ohyashiki, Kazuma
|
|
1996
|
89 |
2 |
p. 114-117
4 p.
|
artikel
|
Tijdschrift beschrijving