Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 166

1.

A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6.

Qin N, Bartley J, Wang JC, Warburton PE.

Cytogenet Genome Res. 2007;119(1-2):154-7. Epub 2007 Dec 14.

PMID:
18160796
[PubMed - indexed for MEDLINE]
2.

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. doi: 10.1159/000322815. Epub 2011 Jan 6.

PMID:
21212645
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.

Lasan Trcić R, Hitrec V, Letica L, Cuk M, Begović D.

Croat Med J. 2003 Aug;44(4):477-9.

PMID:
12950153
[PubMed - indexed for MEDLINE]
Free Article
4.

Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment.

Friedman JM, Harrod MJ, Howard-Peebles PN.

Am J Med Genet. 1992 Sep 1;44(1):37-40.

PMID:
1519647
[PubMed - indexed for MEDLINE]
5.

Interstitial deletion 11(p11.12p11.2) and analphoid marker formation results in inherited Potocki-Shaffer syndrome.

Chuang L, Wakui K, Sue WC, Su MH, Shaffer LG, Kuo PL.

Am J Med Genet A. 2005 Mar 1;133A(2):180-3.

PMID:
15666301
[PubMed - indexed for MEDLINE]
6.

A neocentromere on human chromosome 3 without detectable alpha-satellite DNA forms morphologically normal kinetochores.

Wandall A, Tranebjaerg L, Tommerup N.

Chromosoma. 1998 Dec;107(6-7):359-65.

PMID:
9914367
[PubMed - indexed for MEDLINE]
7.

Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype.

Izumi K, Yamashita Y, Aramaki M, Kosaki R, Hosokai N, Takahashi T, Kosaki K.

Am J Med Genet A. 2008 Aug 1;146A(15):1967-71. doi: 10.1002/ajmg.a.32120.

PMID:
18561337
[PubMed - indexed for MEDLINE]
8.

Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.

Engelen JJ, Moog U, Weber J, Haagen AA, van Uum CM, Hamers AJ.

Am J Med Genet A. 2003 Jun 15;119A(3):356-9.

PMID:
12784305
[PubMed - indexed for MEDLINE]
9.

Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report.

Brisset S, Izard V, Misrahi M, Aboura A, Madoux S, Ferlicot S, Schoevaert D, Soufir JC, Frydman R, Tachdjian G.

Hum Reprod. 2005 Aug;20(8):2168-72. Epub 2005 Apr 21.

PMID:
15845593
[PubMed - indexed for MEDLINE]
Free Article
10.

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.

PMID:
12627422
[PubMed - indexed for MEDLINE]
11.

Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.

Velinov M, Gu H, Genovese M, Duncan C, Warburton P, Brooks SS, Jenkins EC.

Ann Genet. 2004 Apr-Jun;47(2):199-205.

PMID:
15183754
[PubMed - indexed for MEDLINE]
12.

Interstitial deletion of 6q without phenotypic effect.

Hansson K, Szuhai K, Knijnenburg J, van Haeringen A, de Pater J.

Am J Med Genet A. 2007 Jun 15;143A(12):1354-7.

PMID:
17506100
[PubMed - indexed for MEDLINE]
13.

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.

PMID:
14512964
[PubMed - indexed for MEDLINE]
Free Article
14.

Minute supernumerary marker chromosomes identified in two patients with a related, larger pseudodicentric chromosome.

Tung G, Covert SM, Malabed KL, Wohlferd MM, Beckerman KP, Goldberg JD, Cotter PD.

Am J Med Genet. 2001 Oct 15;103(3):193-7.

PMID:
11745990
[PubMed - indexed for MEDLINE]
15.

Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.

Mdzin R, Ko C, Abdul Latif Z, Zakaria Z.

Singapore Med J. 2008 Nov;49(11):e336-9.

PMID:
19037546
[PubMed - indexed for MEDLINE]
Free Article
16.

A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

Mackie Ogilvie C, Harrison RH, Horsley SW, Hodgson SV, Kearney L.

Cytogenet Cell Genet. 2001;92(1-2):69-73.

PMID:
11306799
[PubMed - indexed for MEDLINE]
17.

A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.

Gimelli G, Giorda R, Beri S, Gimelli S, Zuffardi O.

Eur J Med Genet. 2007 Jul-Aug;50(4):264-73. Epub 2007 May 6.

PMID:
17567547
[PubMed - indexed for MEDLINE]
18.

A new neocentromere locus on chromosome 13 resulting in mosaic tetrasomy for distal 13q and an asymmetric phenotype.

Barwell J, Mazzaschi R, Bint S, Ogilvie CM, Elmslie F.

Am J Med Genet A. 2004 Oct 15;130A(3):295-8. Review.

PMID:
15378552
[PubMed - indexed for MEDLINE]
19.

A de novo interstitial deletion of chromosome 6 (q22.2q23.1).

Park JP, Graham JM Jr, Berg SZ, Wurster-Hill DH.

Clin Genet. 1988 Feb;33(2):65-8.

PMID:
3359667
[PubMed - indexed for MEDLINE]
20.

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.

PMID:
10593999
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk