532 related articles for article (PubMed ID: 7802042)
1. 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]
2. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.
Callen DF; Eyre H; Yip MY; Freemantle J; Haan EA
Am J Med Genet; 1992 Jul; 43(4):709-15. PubMed ID: 1377870
[TBL] [Abstract][Full Text] [Related]
5. Identification of supernumerary der(20) chromosomes by FISH in three patients.
Viersbach R; Engels H; Schwanitz G
Am J Med Genet; 1997 Jun; 70(3):278-83. PubMed ID: 9188666
[TBL] [Abstract][Full Text] [Related]
6. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT
Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446
[TBL] [Abstract][Full Text] [Related]
7. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
8. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
González-del-Angel A; Blanco B; del Castillo V; Carnevale A
Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
[TBL] [Abstract][Full Text] [Related]
9. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
10. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
11. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
13. Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twins.
Shanske AL; Dowling P; Schmidt R; White BJ; Russell B; Bogdanow A; Marion RW
J Med Genet; 1999 Aug; 36(8):625-8. PubMed ID: 10465114
[TBL] [Abstract][Full Text] [Related]
14. Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.
Pezzolo A; Perroni L; Gimelli G; Arslanian A; Porta S; Gandullia P; Gandullia E
Ann Genet; 1993; 36(2):121-5. PubMed ID: 8215218
[TBL] [Abstract][Full Text] [Related]
15. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
[TBL] [Abstract][Full Text] [Related]
16. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
Lin CC; Meyne J; Sasi R; Bowen P; Unger T; Tainaka T; Hadro TA; Hoo JJ
Am J Med Genet; 1990 Sep; 37(1):71-8. PubMed ID: 2240047
[TBL] [Abstract][Full Text] [Related]
20. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]