128 related articles for article (PubMed ID: 11494970)
1. A supernumerary marker chromosome with a neocentromere derived from 5p14-->pter.
Fritz B; Dietze I; Wandall A; Aslan M; Schmidt A; Kattner E; Schwerdtfeger R; Friedrich U
J Med Genet; 2001 Aug; 38(8):559-65. PubMed ID: 11494970
[No Abstract] [Full Text] [Related]
2. Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association.
Kumar MJ; Kumar RA; Subhashree V; Jayasudha T; Hemagowri V; Koshy T; Gowrishankar K
Cytogenet Genome Res; 2015; 146(2):120-123. PubMed ID: 26226839
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Oculoauriculovertebral spectrum with 5p15.33-pter deletion.
Descartes M
Clin Dysmorphol; 2006 Jul; 15(3):153-154. PubMed ID: 16760734
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicism.
Engel U; Bohlander SK; Bink K; Hinney B; Laccone F; Bartels I
Hum Reprod; 2001 Jan; 16(1):63-66. PubMed ID: 11139538
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
Tonnies H; Gerlach A; Heineking B; Starke H; Neitzel H; Neumann LM
Cytogenet Genome Res; 2006; 114(3-4):325-9. PubMed ID: 16954674
[TBL] [Abstract][Full Text] [Related]
9. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
D'Amato Sizonenko L; Ng D; Oei P; Winship I
Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
[TBL] [Abstract][Full Text] [Related]
10. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
[TBL] [Abstract][Full Text] [Related]
11. Identification of an unusual marker chromosome by spectral karyotyping.
Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
[TBL] [Abstract][Full Text] [Related]
12. De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISH.
Sanchez-Garcia JF; de Die-Smulders CE; Weber JW; Jetten AG; Loneus WH; Hamers AJ; Engelen JJ
Am J Med Genet; 2001 Apr; 100(1):56-61. PubMed ID: 11337750
[TBL] [Abstract][Full Text] [Related]
13. Centromeric association of chromosome 16- and 18-derived microchromosomes.
Felbor U; Rutschow D; Haaf T; Schmid M
Hum Genet; 2002 Jul; 111(1):16-25. PubMed ID: 12136231
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy 22 in a liveborn resulting from a rearrangement between chromosomes 6 and 22.
Mirza G; Imaizumi K; Ragoussis J
J Med Genet; 2000 Sep; 37(9):E22. PubMed ID: 10978369
[No Abstract] [Full Text] [Related]
15. 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; 133A(2):180-3. PubMed ID: 15666301
[TBL] [Abstract][Full Text] [Related]
16. 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; 130A(3):295-8. PubMed ID: 15378552
[TBL] [Abstract][Full Text] [Related]
17. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
Tatar A; Oztas S; Yakut T; Ors R
Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
Louvrier C; Egea G; Labalme A; Des Portes V; Gazzo S; Callet-Bauchu E; Till M; Sanlaville D; Edery P; Schluth-Bolard C
Cytogenet Genome Res; 2015; 147(2-3):111-7. PubMed ID: 26669311
[TBL] [Abstract][Full Text] [Related]
19. Supernumerary ring chromosome 5 identified by FISH.
Masuno M; Imaizumi K; Ishii T; Kimura J; Kuroki Y
Am J Med Genet; 1999 Jun; 84(4):381. PubMed ID: 10340657
[No Abstract] [Full Text] [Related]
20. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]