265 related articles for article (PubMed ID: 12116235)
41. Molecular cytogenetic characterization of pancreas cancer cell lines reveals high complexity chromosomal alterations.
Griffin CA; Morsberger L; Hawkins AL; Haddadin M; Patel A; Ried T; Schrock E; Perlman EJ; Jaffee E
Cytogenet Genome Res; 2007; 118(2-4):148-56. PubMed ID: 18000365
[TBL] [Abstract][Full Text] [Related]
42. Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysis.
Luquet I; Favre B; Nadal N; Madinier N; Khau Van Kien P; Huet F; Nivelon-Chevallier A; Mugneret F
Ann Genet; 1999; 42(1):33-9. PubMed ID: 10214505
[TBL] [Abstract][Full Text] [Related]
43. Class II neocentromeres: a putative common neocentromere site in band 4q21.2.
Warburton PC; Barwell J; Splitt M; Maxwell D; Bint S; Ogilvie CM
Eur J Hum Genet; 2003 Oct; 11(10):749-53. PubMed ID: 14512964
[TBL] [Abstract][Full Text] [Related]
44. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
[TBL] [Abstract][Full Text] [Related]
45. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.
Sawyer JR; Swanson CM; Wheeler G; Cunniff C
Am J Med Genet; 1995 Mar; 56(2):203-9. PubMed ID: 7625446
[TBL] [Abstract][Full Text] [Related]
46. Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
Lillington DM; Kingston JE; Coen PG; Price E; Hungerford J; Domizio P; Young BD; Onadim Z
Genes Chromosomes Cancer; 2003 Feb; 36(2):121-8. PubMed ID: 12508240
[TBL] [Abstract][Full Text] [Related]
47. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
Petty EM; Gibson LH; Breg WR; Burns JP; Yang-Feng TL
Am J Med Genet; 1993 Mar; 45(6):770-3. PubMed ID: 8456860
[TBL] [Abstract][Full Text] [Related]
48. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
[TBL] [Abstract][Full Text] [Related]
49. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
[TBL] [Abstract][Full Text] [Related]
50. Interstitial deletion of proximal 8q including part of the centromere from unbalanced segregation of a paternal deletion/marker karyotype with neocentromere formation at 8p22.
Burnside RD; Ibrahim J; Flora C; Schwartz S; Tepperberg JH; Papenhausen PR; Warburton PE
Cytogenet Genome Res; 2011; 132(4):227-32. PubMed ID: 21212645
[TBL] [Abstract][Full Text] [Related]
51. Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres.
Hasson D; Alonso A; Cheung F; Tepperberg JH; Papenhausen PR; Engelen JJ; Warburton PE
Chromosoma; 2011 Dec; 120(6):621-32. PubMed ID: 21826412
[TBL] [Abstract][Full Text] [Related]
52. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
Rossi E; Riegel M; Messa J; Gimelli S; Maraschio P; Ciccone R; Stroppi M; Riva P; Perrotta CS; Mattina T; Memo L; Baumer A; Kucinskas V; Castellan C; Schinzel A; Zuffardi O
J Med Genet; 2008 Mar; 45(3):147-54. PubMed ID: 18006671
[TBL] [Abstract][Full Text] [Related]
53. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
54. [Identification of the origin of marker chromosome by comparative genomic hybridization].
Zhou L; Wu LQ; Liang DS; Pan Q; Long ZG; Dai HP; Li J; Cai F; Xia K; Xia JH
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):264-7. PubMed ID: 17478934
[TBL] [Abstract][Full Text] [Related]
55. A 330 kb CENP-A binding domain and altered replication timing at a human neocentromere.
Lo AW; Craig JM; Saffery R; Kalitsis P; Irvine DV; Earle E; Magliano DJ; Choo KH
EMBO J; 2001 Apr; 20(8):2087-96. PubMed ID: 11296241
[TBL] [Abstract][Full Text] [Related]
56. dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome.
Davidsson J; Jahnke K; Forsgren M; Collin A; Soller M
Obesity (Silver Spring); 2010 Mar; 18(3):580-7. PubMed ID: 19763090
[TBL] [Abstract][Full Text] [Related]
57. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
58. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
59. A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.
Eussen BH; van de Laar I; Douben H; van Kempen L; Hochstenbach R; De Man SA; Van Opstal D; de Klein A; Poddighe PJ
Eur J Med Genet; 2007; 50(2):112-9. PubMed ID: 17161033
[TBL] [Abstract][Full Text] [Related]
60. Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.
Gravholt CH; Friedrich U
Am J Med Genet; 1995 Mar; 56(1):106-11. PubMed ID: 7747772
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
