208 related articles for article (PubMed ID: 23017438)
1. Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.
Guediche N; Tosca L; Nouchy M; Lecerf L; Cornet D; Brisset S; Goossens M; Tachdjian G
Eur J Med Genet; 2012 Dec; 55(12):737-42. PubMed ID: 23017438
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[TBL] [Abstract][Full Text] [Related]
4. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A small supernumerary marker chromosome, derived from chromosome 22, possibly associated with repeated spontaneous abortions.
Balkan M; Isi H; Gedik A; Erdemoğlu M; Budak T
Genet Mol Res; 2010 Aug; 9(3):1683-9. PubMed ID: 20799165
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
9. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Santos M; Mrasek K; Rigola MA; Starke H; Liehr T; Fuster C
Fertil Steril; 2007 Oct; 88(4):969.e11-7. PubMed ID: 17451694
[TBL] [Abstract][Full Text] [Related]
10. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.
Mrasek K; Starke H; Liehr T
J Histochem Cytochem; 2005 Mar; 53(3):367-70. PubMed ID: 15750022
[TBL] [Abstract][Full Text] [Related]
11. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
Liehr T; Starke H; Senger G; Melotte C; Weise A; Vermeesch JR
Am J Med Genet A; 2006 Jan; 140(1):46-51. PubMed ID: 16333826
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.
Chen CP; Chen M; Wang PT; Chern SR; Chen SW; Lai ST; Wu PS; Chang SP; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Jun; 56(3):394-397. PubMed ID: 28600058
[TBL] [Abstract][Full Text] [Related]
13. Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face.
Sarri C; Gyftodimou Y; Grigoriadou M; Pandelia E; Kalogirou S; Kokotas H; Mrasek K; Weise A; Petersen MB
Cytogenet Genome Res; 2006; 114(3-4):330-7. PubMed ID: 16954675
[TBL] [Abstract][Full Text] [Related]
14. dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome.
Davidsson J; Jahnke K; Forsgren M; Collin A; Soller M
Obesity (Silver Spring); 2010 Mar; 18(3):580-7. PubMed ID: 19763090
[TBL] [Abstract][Full Text] [Related]
15. Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility.
Guediche N; Tosca L; Kara Terki A; Bas C; Lecerf L; Young J; Briand-Suleau A; Tou B; Bouligand J; Brisset S; Misrahi M; Guiochon-Mantel A; Goossens M; Tachdjian G
Reprod Biomed Online; 2012 Jan; 24(1):72-82. PubMed ID: 22116069
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
[TBL] [Abstract][Full Text] [Related]
17. The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype.
Santacroce R; Trunzo R; Leccese A; Pansini A; Gentile M; Margaglione M
Syst Biol Reprod Med; 2015; 61(6):398-402. PubMed ID: 26270802
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
[TBL] [Abstract][Full Text] [Related]
19. Characterization of sSMC by FISH and molecular techniques.
Sheth F; Andrieux J; Ewers E; Kosyakova N; Weise A; Sheth H; Romana SP; LeLorc'h M; Delobel B; Theisen O; Liehr T; Nampoothiri S; Sheth J
Eur J Med Genet; 2011; 54(3):247-55. PubMed ID: 21316495
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.
Marle N; Martinet D; Aboura A; Joly-Helas G; Andrieux J; Flori E; Puechberty J; Vialard F; Sanlaville D; Fert Ferrer S; Bourrouillou G; Tabet AC; Quilichini B; Simon-Bouy B; Bazin A; Becker M; Stora H; Amblard S; Doco-Fenzy M; Molina Gomes D; Girard-Lemaire F; Cordier MP; Satre V; Schneider A; Lemeur N; Chambon P; Jacquemont S; Fellmann F; Vigouroux-Castera A; Molignier R; Delaye A; Pipiras E; Liquier A; Rousseau T; Mosca AL; Kremer V; Payet M; Rangon C; Mugneret F; Aho S; Faivre L; Callier P
Clin Genet; 2014 Mar; 85(3):233-44. PubMed ID: 23489061
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
