112 related articles for article (PubMed ID: 20029167)
1. First case of a neocentromere formation in an otherwise normal chromosome 7.
Liehr T; Kosyakova N; Weise A; Ziegler M; Raabe-Meyer G
Cytogenet Genome Res; 2010 Jun; 128(4):189-91. PubMed ID: 20029167
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
[TBL] [Abstract][Full Text] [Related]
4. Trisomy 20p resulting from inverted duplication and neocentromere formation.
Voullaire L; Saffery R; Davies J; Earle E; Kalitsis P; Slater H; Irvine DV; Choo KH
Am J Med Genet; 1999 Aug; 85(4):403-8. PubMed ID: 10398268
[TBL] [Abstract][Full Text] [Related]
5. Neocentromere formation in a stable ring 1p32-p36.1 chromosome.
Slater HR; Nouri S; Earle E; Lo AW; Hale LG; Choo KH
J Med Genet; 1999 Dec; 36(12):914-8. PubMed ID: 10593999
[TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.
Warburton PE; Dolled M; Mahmood R; Alonso A; Li S; Naritomi K; Tohma T; Nagai T; Hasegawa T; Ohashi H; Govaerts LC; Eussen BH; Van Hemel JO; Lozzio C; Schwartz S; Dowhanick-Morrissette JJ; Spinner NB; Rivera H; Crolla JA; Yu C; Warburton D
Am J Hum Genet; 2000 Jun; 66(6):1794-806. PubMed ID: 10777715
[TBL] [Abstract][Full Text] [Related]
7. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
[TBL] [Abstract][Full Text] [Related]
8. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
[TBL] [Abstract][Full Text] [Related]
9. Evolutionary new centromeres in primates.
Rocchi M; Stanyon R; Archidiacono N
Prog Mol Subcell Biol; 2009; 48():103-52. PubMed ID: 19521814
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Phylogeny of horse chromosome 5q in the genus Equus and centromere repositioning.
Piras FM; Nergadze SG; Poletto V; Cerutti F; Ryder OA; Leeb T; Raimondi E; Giulotto E
Cytogenet Genome Res; 2009; 126(1-2):165-72. PubMed ID: 20016166
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetic characterization of a metastatic lung sarcomatoid carcinoma: 9p23 neocentromere and 9p23-p24 amplification including JAK2 and JMJD2C.
Italiano A; Attias R; Aurias A; Pérot G; Burel-Vandenbos F; Otto J; Venissac N; Pedeutour F
Cancer Genet Cytogenet; 2006 Jun; 167(2):122-30. PubMed ID: 16737911
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
Michalski K; Rauer M; Williamson N; Perszyk A; Hoo JJ
Am J Med Genet; 1993 Apr; 46(1):88-94. PubMed ID: 8494036
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
Knegt AC; Li S; Engelen JJ; Bijlsma EK; Warburton PE
Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
Perfumo C; Arslanian A; Zara F; Piombo G; Pierluigi M
Pathologica; 1992; 84(1091):363-9. PubMed ID: 1465321
[TBL] [Abstract][Full Text] [Related]
19. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
[TBL] [Abstract][Full Text] [Related]
20. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]