225 related articles for article (PubMed ID: 16103662)
21. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
[TBL] [Abstract][Full Text] [Related]
22. Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.
Manvelyan M; Riegel M; Santos M; Fuster C; Pellestor F; Mazaurik ML; Schulze B; Polityko A; Tittelbach H; Reising-Ackermann G; Belitz B; Hehr U; Kelbova C; Volleth M; Gödde E; Anderson J; Küpferling P; Köhler S; Duba HC; Dufke A; Aktas D; Martin T; Schreyer I; Ewers E; Reich D; Mrasek K; Weise A; Liehr T
Int J Mol Med; 2008 Jun; 21(6):705-14. PubMed ID: 18506363
[TBL] [Abstract][Full Text] [Related]
23. Small supernumerary marker chromosomes (sSMC) in humans.
Liehr T; Claussen U; Starke H
Cytogenet Genome Res; 2004; 107(1-2):55-67. PubMed ID: 15305057
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
Fickelscher I; Starke H; Schulze E; Ernst G; Kosyakova N; Mkrtchyan H; MacDermont K; Sebire N; Liehr T
Prenat Diagn; 2007 Aug; 27(8):783-5. PubMed ID: 17546703
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2).
Li T; Xue Y; Zhang J; Chen S; Pan J; Wu Y; Wang Y; Shen J
Cancer Genet Cytogenet; 2008 Feb; 181(1):55-9. PubMed ID: 18262055
[TBL] [Abstract][Full Text] [Related]
29. Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.
Klein E; Rocchi M; Ovens-Raeder A; Kosyakova N; Weise A; Ziegler M; Meins M; Morlot S; Fischer W; Volleth M; Polityko A; Ogilvie CM; Kraus C; Liehr T
Cytogenet Genome Res; 2012; 136(3):163-6. PubMed ID: 22377933
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
Liehr T
Methods Mol Biol; 2008; 444():27-38. PubMed ID: 18425469
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.
Vraneković J; Brajenović-Milić B; Modrusan-Mozetić Z; Babić I; Kapović M
Cytogenet Genome Res; 2008; 121(3-4):298-301. PubMed ID: 18758176
[TBL] [Abstract][Full Text] [Related]
34. Familial small supernumerary marker chromosome (sSMC) (14)(:p11-q11:) [corrected] in a child with translocation Down syndrome.
Vundinti BR; Korgaonkar S; Ghosh K
Indian J Pediatr; 2009 Dec; 76(12):1265-7. PubMed ID: 20012787
[TBL] [Abstract][Full Text] [Related]
35. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
[TBL] [Abstract][Full Text] [Related]
36. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
Manolakos E; Kefalas K; Neroutsou R; Lagou M; Kosyakova N; Ewers E; Ziegler M; Weise A; Tsoplou P; Rapti SM; Papoulidis I; Anastasakis E; Garas A; Sotiriou S; Eleftheriades M; Peitsidis P; Malathrakis D; Thomaidis L; Kitsos G; Orru S; Liehr T; Petersen MB; Kitsiou-Tzeli S
Mol Med Rep; 2010; 3(6):1015-22. PubMed ID: 21472348
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
[TBL] [Abstract][Full Text] [Related]
39. Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.
Chen CP; Chen M; Su YN; Huang JP; Chern SR; Wu PS; Su JW; Chang SP; Chen YT; Lee CC; Chen LF; Pan CW; Wang W
Gene; 2013 Oct; 529(1):169-75. PubMed ID: 23933412
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]