199 related articles for article (PubMed ID: 18758176)
1. 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]
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. 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]
4. 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]
5. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
[TBL] [Abstract][Full Text] [Related]
6. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
[TBL] [Abstract][Full Text] [Related]
11. Duplication of distal 19q: clinical report and review.
Boyd E; Grass FS; Parke JC; Knutson K; Stevenson RE
Am J Med Genet; 1992 Feb; 42(3):326-30. PubMed ID: 1536172
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
14. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
[TBL] [Abstract][Full Text] [Related]
15. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Vundinti BR; Korgaonkar S; Ghosh K
Gene; 2012 Apr; 498(1):128-30. PubMed ID: 22342255
[TBL] [Abstract][Full Text] [Related]
18. Supernumerary chromosome marker (1) in a developmentally delayed child.
Lanphear N; Lamb A; Oppenheimer S; Soukup S
Am J Med Genet; 1995 Jul; 57(3):400-2. PubMed ID: 7545867
[TBL] [Abstract][Full Text] [Related]
19. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
[TBL] [Abstract][Full Text] [Related]
20. Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.
Stankiewicz P; Bocian E; Jakubów-Durska K; Obersztyn E; Lato E; Starke H; Mroczek K; Mazurczak T
J Med Genet; 2000 Feb; 37(2):114-20. PubMed ID: 10662811
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
