153 related articles for article (PubMed ID: 7542834)
1. Marker chromosome 21 identified by microdissection and FISH.
Sun Y; Rubinstein J; Soukup S; Palmer CG
Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ
Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122
[TBL] [Abstract][Full Text] [Related]
4. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
5. Duplication 20p identified via fluorescent in situ hybridization.
LeChien KA; McPherson E; Estop AM
Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. 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]
9. 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]
10. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
[TBL] [Abstract][Full Text] [Related]
12. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.
Tonk V; Schneider NR; Delgado MR; Mao J; Schultz RA
Am J Med Genet; 1996 Jan; 61(1):16-20. PubMed ID: 8741911
[TBL] [Abstract][Full Text] [Related]
13. Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH.
Engelen JJ; Tuerlings JH; Albrechts JC; Schrander-Stumpel CT; Hamers AJ; De Die-Smulders CE
Genet Couns; 2000; 11(1):13-7. PubMed ID: 10756422
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ
Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. 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]
[Next] [New Search]