167 related articles for article (PubMed ID: 25774219)
1. Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome.
Ma R; Peng Y; Zhang Y; Xia Y; Tang G; Chang J; Guo R; Gui B; Huang Y; Chen C; Liang D; Wu L
Mol Cytogenet; 2015; 8():10. PubMed ID: 25774219
[TBL] [Abstract][Full Text] [Related]
2. De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review.
Syu YM; Ma JY; Ou TH; Lee CL; Lin HY; Lin SP; Lee CJ; Chen CP
Diagnostics (Basel); 2022 Sep; 12(10):. PubMed ID: 36291995
[TBL] [Abstract][Full Text] [Related]
3. A female infant with duplication of chromosome 2q33 to 2q37.3.
Slavotinek AM; Boles D; Lacbawan F
Clin Dysmorphol; 2003 Oct; 12(4):251-6. PubMed ID: 14564213
[TBL] [Abstract][Full Text] [Related]
4. Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Liehr T; Utine GE; Trautmann U; Rauch A; Kuechler A; Pietrzak J; Bocian E; Kosyakova N; Mrasek K; Boduroglu K; Weise A; Aktas D
Cytogenet Genome Res; 2007; 118(1):31-7. PubMed ID: 17901697
[TBL] [Abstract][Full Text] [Related]
5. Case Report: Prenatal Identification of a
Dharmadhikari AV; Pereira EM; Andrews CC; Macera M; Harkavy N; Wapner R; Jobanputra V; Levy B; Ganapathi M; Liao J
Front Genet; 2022; 13():906077. PubMed ID: 35928455
[TBL] [Abstract][Full Text] [Related]
6. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes.
Weber A; Liehr T; Al-Rikabi A; Bilgen S; Heinrich U; Schiller J; Stumm M
Biomedicines; 2022 May; 10(5):. PubMed ID: 35625839
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H
Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833
[TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
11. PARTIAL TRISOMY 5p12-q 11.2 RESULTING FROM A MARKER CHROMOSOME: A NEW CASE REPORT WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER.
Erdem HB; Sahin I; Tasdemir S; Tatar A
Genet Couns; 2016; 27(3):295-303. PubMed ID: 30204959
[TBL] [Abstract][Full Text] [Related]
12. A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype.
Camerota L; Pitzianti M; Postorivo D; Nardone AM; Ligas C; Moretti C; Pasini A; Brancati F
Cytogenet Genome Res; 2017; 153(1):22-28. PubMed ID: 29141250
[TBL] [Abstract][Full Text] [Related]
13. Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array.
Zhou L; Zheng Z; Wu L; Xu C; Wu H; Xu X; Tang S
Mol Cytogenet; 2020; 13():19. PubMed ID: 32514314
[TBL] [Abstract][Full Text] [Related]
14. Complex small supernumerary marker chromosome with a 15q/16p duplication: clinical implications.
Christofolini DM; Piazzon FB; Evo C; Mafra FA; Cosenza SR; Dias AT; Barbosa CP; Bianco B; Kulikowski LD
Mol Cytogenet; 2014; 7():29. PubMed ID: 24839463
[TBL] [Abstract][Full Text] [Related]
15. Small supernumerary marker chromosomes derived from chromosome 14 and/or 22.
Liehr T; Williams HE; Ziegler M; Kankel S; Padutsch N; Al-Rikabi A
Mol Cytogenet; 2021 Feb; 14(1):13. PubMed ID: 33632263
[TBL] [Abstract][Full Text] [Related]
16. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.
Melo JB; Backx L; Vermeesch JR; Santos HG; Sousa AC; Kosyakova N; Weise A; von Eggeling F; Liehr T; Carreira IM
J Appl Genet; 2011 May; 52(2):193-200. PubMed ID: 21437654
[TBL] [Abstract][Full Text] [Related]
17. Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature.
Marchina E; Forti M; Tonelli M; Maccarini S; Malvestiti F; Piantoni C; Filippini E; Fazzi E; Borsani G
Mol Cytogenet; 2021 Jan; 14(1):6. PubMed ID: 33472639
[TBL] [Abstract][Full Text] [Related]
18. Small supernumerary marker chromosomes derived from human chromosome 11.
Liehr T; Ziegler M; Person L; Kankel S; Padutsch N; Weise A; Weimer JP; Williams H; Ferreira S; Melo JB; Carreira IM
Front Genet; 2023; 14():1293652. PubMed ID: 38174048
[No Abstract] [Full Text] [Related]
19. Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes.
Cheng D; Yuan S; Yi D; Luo K; Xu F; Gong F; Lu C; Lu G; Lin G; Tan YQ
J Assist Reprod Genet; 2019 Dec; 36(12):2533-2539. PubMed ID: 31720922
[TBL] [Abstract][Full Text] [Related]
20. A new small supernumerary marker chromosome involving 14pter → q12 in a child with severe neurodevelopmental retardation: case report and literature review.
Qi M; Zhao Y; Wang Y; Li T
Gene; 2013 Dec; 531(2):457-61. PubMed ID: 24013083
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]