101 related articles for article (PubMed ID: 8344672)
21. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
[TBL] [Abstract][Full Text] [Related]
22. Myeloid antigen positive acute lymphoblastic leukemia with the Philadelphia translocation and a jumping translocation of 1q in a child.
Montgomery KD; Winter SS; Frost JD; Hardekopf D; Holt K; Graham ML; Foucar K
Leukemia; 2004 Sep; 18(9):1548-50. PubMed ID: 15284862
[No Abstract] [Full Text] [Related]
23. [Genetic risk of families with t(1;2)(q42;q33) GTG, RHG, QFQ, FISH].
Stasiewicz-Jarocka B; Raczkiewicz B; Kowalczyk D; Zawada M; Midro AT
Ginekol Pol; 2000 Oct; 71(10):1262-72. PubMed ID: 11143935
[TBL] [Abstract][Full Text] [Related]
24. Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7.
Alitalo T; Willard HF; de la Chapelle A
Cytogenet Cell Genet; 1989; 50(1):49-53. PubMed ID: 2743817
[TBL] [Abstract][Full Text] [Related]
25. Identification of a male schizophrenic patient carrying a de novo balanced translocation, t(4; 13)(p16.1; q21.31).
Itokawa M; Kasuga T; Yoshikawa T; Matsushita M
Psychiatry Clin Neurosci; 2004 Jun; 58(3):333-7. PubMed ID: 15149303
[TBL] [Abstract][Full Text] [Related]
26. Regional chromosomal assignment of human renin gene to 1q12----qter and use in linkage studies in Charcot-Marie-Tooth disease.
Griffiths LR; Nicholson GA; Ross DA; Zwi MB; McLeod JG; Mohandas T; Morris BJ
Cytogenet Cell Genet; 1987; 45(3-4):231-3. PubMed ID: 3319438
[TBL] [Abstract][Full Text] [Related]
27. The complex history of distal human chromosome 1q.
Haig D
Genomics; 2005 Dec; 86(6):767-70. PubMed ID: 16293392
[TBL] [Abstract][Full Text] [Related]
28. Jumping translocation of 1q in a BCR/ABL-positive acute lymphoblastic leukemia.
Pelz AF; Müller G; Wieacker P
Cancer Genet Cytogenet; 2005 Mar; 157(2):157-9. PubMed ID: 15721638
[TBL] [Abstract][Full Text] [Related]
29. Chromosome 1 abnormalities in multiple myeloma.
Marzin Y; Jamet D; Douet-Guilbert N; Morel F; Le Bris MJ; Morice P; Abgrall JF; Berthou C; De Braekeleer M
Anticancer Res; 2006; 26(2A):953-9. PubMed ID: 16619492
[TBL] [Abstract][Full Text] [Related]
30. Reassignment of the human CSF1 gene to chromosome 1p13-p21.
Morris SW; Valentine MB; Shapiro DN; Sublett JE; Deaven LL; Foust JT; Roberts WM; Cerretti DP; Look AT
Blood; 1991 Oct; 78(8):2013-20. PubMed ID: 1912583
[TBL] [Abstract][Full Text] [Related]
31. Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31----q32.
Coucke P; Mangelschots K; Speleman F; Bossuyt P; Van Oostveldt P; Van der Auwera B; Carritt B; Willems PJ
Cytogenet Cell Genet; 1991; 57(2-3):120-2. PubMed ID: 1914520
[TBL] [Abstract][Full Text] [Related]
32. Trisomy (1q)(q42----qter): confirmation of a syndrome.
Chia NL; Bousfield LR; Poon CC; Trudinger BJ
Clin Genet; 1988 Oct; 34(4):224-9. PubMed ID: 3233776
[TBL] [Abstract][Full Text] [Related]
33. [Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH].
Sawicka A; Leśniewicz R; Zawada M; Stasiewicz-Jarocka B; Midro AT
Ginekol Pol; 1998 Apr; 69(4):200-6. PubMed ID: 9640866
[TBL] [Abstract][Full Text] [Related]
34. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
Mewar R; Kline AD; Jackson L; Overhauser J
Am J Med Genet; 1992 Nov; 44(4):477-81. PubMed ID: 1442891
[TBL] [Abstract][Full Text] [Related]
35. Translocation (8;14)(q24;q32) as the sole cytogenetic abnormality in B-cell prolymphocytic leukemia.
Kuriakose P; Perveen N; Maeda K; Wiktor A; Van Dyke DL
Cancer Genet Cytogenet; 2004 Apr; 150(2):156-8. PubMed ID: 15066324
[TBL] [Abstract][Full Text] [Related]
36. Identification of complex chromosome rearrangements in the gibbon by fluorescent in situ hybridization (FISH) of a human chromosome 2q specific microlibrary, yeast artificial chromosomes, and reciprocal chromosome painting.
Arnold N; Stanyon R; Jauch A; O'Brien P; Wienberg J
Cytogenet Cell Genet; 1996; 74(1-2):80-5. PubMed ID: 8893807
[TBL] [Abstract][Full Text] [Related]
37. Jumping translocation in a case of de novo infant acute myeloid leukemia.
Parihar M; Gupta A; Yadav AK; Mishra DK; Bhattacharyya A; Chandy M
Pediatr Blood Cancer; 2014 Feb; 61(2):387-9. PubMed ID: 24019227
[TBL] [Abstract][Full Text] [Related]
38. Translocation junctions cluster at the distal short arm of chromosome 1 (1p36.1-2) in human neuroblastoma cells.
Barker PE; Savelyeva L; Schwab M
Oncogene; 1993 Dec; 8(12):3353-8. PubMed ID: 8247537
[TBL] [Abstract][Full Text] [Related]
39. Regional localization of the human genes for malate dehydrogenase-1 and isocitrate dehydrogenase-1 on chromosome 2 by interspecific hybridization using human cells with the balanced reciprocal translocation t(1;2) (q32;q13).
Francke U
Cytogenet Cell Genet; 1975; 14(3-6):308-12. PubMed ID: 1192808
[No Abstract] [Full Text] [Related]
40. Chromosomal mapping of human angiotensinogen gene and human renin gene by fluorescence in situ hybridization (FISH) in transgenic mice.
Watanabe Y; Ebukuro M; Yagami K; Sugiyama F; Ishida J; Murakami K; Nomura T; Katoh H
Exp Anim; 1996 Jul; 45(3):265-9. PubMed ID: 8840145
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
