169 related articles for article (PubMed ID: 15044915)
1. Cytogenetic and molecular cytogenetic findings in 43 aneurysmal bone cysts: aberrations of 17p mapped to 17p13.2 by fluorescence in situ hybridization.
Althof PA; Ohmori K; Zhou M; Bailey JM; Bridge RS; Nelson M; Neff JR; Bridge JA
Mod Pathol; 2004 May; 17(5):518-25. PubMed ID: 15044915
[TBL] [Abstract][Full Text] [Related]
2. Aberrations of 6q13 mapped to the COL12A1 locus in chondromyxoid fibroma.
Yasuda T; Nishio J; Sumegi J; Kapels KM; Althof PA; Sawyer JR; Reith JD; Bridge JA
Mod Pathol; 2009 Nov; 22(11):1499-506. PubMed ID: 19648885
[TBL] [Abstract][Full Text] [Related]
3. Aneurysmal bone cyst of the nose with 17p13 involvement.
Winnepenninckx V; Debiec-Rychter M; Jorissen M; Bogaerts S; Sciot R
Virchows Arch; 2001 Nov; 439(5):636-9. PubMed ID: 11764383
[TBL] [Abstract][Full Text] [Related]
4. Fusion of the Lumican (
Panagopoulos I; Gorunova L; Andersen K; Lobmaier I; Lund-Iversen M; Micci F; Heim S
Cancer Genomics Proteomics; 2020; 17(5):555-561. PubMed ID: 32859633
[TBL] [Abstract][Full Text] [Related]
5. Translocation (16;17)(q22;p13) is a recurrent anomaly of aneurysmal bone cysts.
Herens C; Thiry A; Dresse MF; Born J; Flagothier C; Vanstraelen G; Allington N; Bex V
Cancer Genet Cytogenet; 2001 May; 127(1):83-4. PubMed ID: 11408073
[TBL] [Abstract][Full Text] [Related]
6. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p.
Baruffi MR; Neto JB; Barbieri CH; Casartelli C
Cancer Genet Cytogenet; 2001 Sep; 129(2):177-80. PubMed ID: 11566352
[TBL] [Abstract][Full Text] [Related]
7. Recurrent t(16;17)(q22;p13) in aneurysmal bone cysts.
Panoutsakopoulos G; Pandis N; Kyriazoglou I; Gustafson P; Mertens F; Mandahl N
Genes Chromosomes Cancer; 1999 Nov; 26(3):265-6. PubMed ID: 10502326
[TBL] [Abstract][Full Text] [Related]
8. Two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20.
Descipio C; Morrissette JD; Conlin LK; Clark D; Kaur M; Coplan J; Riethman H; Spinner NB; Krantz ID
Am J Med Genet A; 2010 Feb; 152A(2):373-82. PubMed ID: 20101690
[TBL] [Abstract][Full Text] [Related]
9. Identification of a commonly deleted region at 17p13.3 in leukemia and lymphoma associated with 17p abnormality.
Sankar M; Tanaka K; Kumaravel TS; Arif M; Shintani T; Yagi S; Kyo T; Dohy H; Kamada N
Leukemia; 1998 Apr; 12(4):510-6. PubMed ID: 9557609
[TBL] [Abstract][Full Text] [Related]
10. Unknown partner for USP6 and unusual SS18 rearrangement detected by fluorescence in situ hybridization in a solid aneurysmal bone cyst.
Geiersbach K; Rector LS; Sederberg M; Hooker A; Randall RL; Schiffman JD; South ST
Cancer Genet; 2011 Apr; 204(4):195-202. PubMed ID: 21536237
[TBL] [Abstract][Full Text] [Related]
11. High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.
Scheurlen WG; Seranski P; Mincheva A; Kühl J; Sörensen N; Krauss J; Lichter P; Poustka A; Wilgenbus KK
Genes Chromosomes Cancer; 1997 Jan; 18(1):50-8. PubMed ID: 8993980
[TBL] [Abstract][Full Text] [Related]
12. Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group.
Sciot R; Dorfman H; Brys P; Dal Cin P; De Wever I; Fletcher CD; Jonson K; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Samson I; Tallini G; Van den Berghe H; Vanni R; Willén H
Mod Pathol; 2000 Nov; 13(11):1206-10. PubMed ID: 11106078
[TBL] [Abstract][Full Text] [Related]
13. Primary aneurysmal bone cysts: 16q22 and/or 17p13 chromosome abnormalities.
Wyatt-Ashmead J; Bao L; Eilert RE; Gibbs P; Glancy G; McGavran L
Pediatr Dev Pathol; 2001; 4(4):418-9. PubMed ID: 11441369
[No Abstract] [Full Text] [Related]
14. Miller-Dieker syndrome with der(17)t(12;17)(q24.33;p13.3)pat presenting with a potential risk of mis-identification as a de novo submicroscopic deletion of 17p13.3.
Kim YJ; Byun SY; Jo SA; Shin YB; Cho EH; Lee EY; Hwang SH
Korean J Lab Med; 2011 Jan; 31(1):49-53. PubMed ID: 21239872
[TBL] [Abstract][Full Text] [Related]
15. Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring.
Alvarado M; Bass HN; Caldwell S; Jamehdor M; Miller AA; Jacob P
Am J Dis Child; 1993 Dec; 147(12):1291-4. PubMed ID: 8249946
[TBL] [Abstract][Full Text] [Related]
16. Cytogenetic and molecular cytogenetic analysis of B cell chronic lymphocytic leukemia: specific chromosome aberrations identify prognostic subgroups of patients and point to loci of candidate genes.
Döhner H; Stilgenbauer S; Fischer K; Bentz M; Lichter P
Leukemia; 1997 Apr; 11 Suppl 2():S19-24. PubMed ID: 9178833
[TBL] [Abstract][Full Text] [Related]
17. [Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome].
Lin S; Luo Y; Wu J; Chen B; Ji Y; Zhou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):89-92. PubMed ID: 28186603
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a complex chromosome rearrangement involving 6q in a melanoma cell line by chromosome microdissection.
Guan XY; Zhang HE; Zhou H; Sham JS; Fung JM; Trent JM
Cancer Genet Cytogenet; 2002 Apr; 134(1):65-70. PubMed ID: 11996799
[TBL] [Abstract][Full Text] [Related]
19. Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.
Vissers LE; Stankiewicz P; Yatsenko SA; Crawford E; Creswick H; Proud VK; de Vries BB; Pfundt R; Marcelis CL; Zackowski J; Bi W; van Kessel AG; Lupski JR; Veltman JA
Hum Genet; 2007 Jul; 121(6):697-709. PubMed ID: 17457615
[TBL] [Abstract][Full Text] [Related]
20. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients.
Hurd LM; Thacker MM; Okenfuss E; Duker AL; Lou Y; Harty MP; Conard K; Lian JB; Bober MB
Am J Med Genet A; 2017 Dec; 173(12):3205-3210. PubMed ID: 29080333
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
