326 related articles for article (PubMed ID: 12655496)
1. SKY assessment of two karyotypes with 0-6 supernumerary marker/ring chromosomes and review of previously reported cases with two or more markers.
Reddy KS; Wang S; Groh S; Gonatos J
Am J Med Genet A; 2003 Apr; 118A(2):156-71. PubMed ID: 12655496
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Identification of marker chromosomes in thirteen patients using FISH probing.
Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
[TBL] [Abstract][Full Text] [Related]
4. A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15.
Daniel A; Malafiej P
Am J Med Genet A; 2003 Mar; 117A(3):212-22. PubMed ID: 12599184
[TBL] [Abstract][Full Text] [Related]
5. A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker.
Dutta UR; Vempally S; Ranganath P; Dalal A
Gene; 2014 Apr; 539(1):162-7. PubMed ID: 24508374
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mosaic trisomy of a small r(1) with an abnormal phenotype.
Dawson AJ; Konkin D; Riordan D; Chudley AE
Am J Med Genet; 2001 Sep; 103(1):32-5. PubMed ID: 11562931
[TBL] [Abstract][Full Text] [Related]
8. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
[TBL] [Abstract][Full Text] [Related]
9. Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.
van Langen IM; Otter MA; Aronson DC; Overweg-Plandsoen WC; Hennekam RC; Leschot NJ; Hoovers JM
Clin Genet; 1996 Jan; 49(1):49-53. PubMed ID: 8721573
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.
Pietrzak J; Mrasek K; Obersztyn E; Stankiewicz P; Kosyakova N; Weise A; Cheung SW; Cai WW; von Eggeling F; Mazurczak T; Bocian E; Liehr T
J Appl Genet; 2007; 48(2):167-75. PubMed ID: 17495351
[TBL] [Abstract][Full Text] [Related]
12. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
[TBL] [Abstract][Full Text] [Related]
13. Supernumerary der(1) marker chromosome derived from a ring chromosome 1 which has retained the original centromere and euchromatin from 1q21.1 --> q21.3 with substantial loss of 1q12 heterochromatin in a female with dysmorphic features and psychomotoric developmental delay.
Barbi G; Spaich Ch; Adolph S; Rossier E; Kehrer-Sawatzki H
Am J Med Genet A; 2005 Feb; 132A(4):419-24. PubMed ID: 15633178
[TBL] [Abstract][Full Text] [Related]
14. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature.
Velagaleti GV; Jalal SM; Kukolich MK; Lockhart LH; Tonk VS
Clin Genet; 2002 Mar; 61(3):202-6. PubMed ID: 12000362
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
von Beust G; Sauter SM; Liehr T; Burfeind P; Bartels I; Starke H; von Eggeling F; Zoll B
Am J Med Genet A; 2005 Aug; 137(1):59-64. PubMed ID: 16007665
[TBL] [Abstract][Full Text] [Related]
18. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of minute supernumerary marker chromosomes.
Cotter PD; Drexler K; Corley AL; Covert SM; Moland JS; Govberg IJ; Norton ME
Gynecol Obstet Invest; 2005; 60(1):27-38. PubMed ID: 15689640
[TBL] [Abstract][Full Text] [Related]
20. A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome.
Pacanaro AN; Christofolini DM; Kulikowski LD; Belangero SI; da Silva Bellucco FT; Varela MC; Koiffmann CP; Yoshimoto M; Squire JA; Schiavon AV; Heck B; Melaragno MI
Am J Med Genet A; 2010 Mar; 152A(3):753-8. PubMed ID: 20186782
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]