110 related articles for article (PubMed ID: 7847800)
1. Tetrasomy 18p in two cases confirmation by in situ hybridization.
Esmer MC; Frias S; Gómez L; Carnevale A
Ann Genet; 1994; 37(3):156-9. PubMed ID: 7847800
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
[TBL] [Abstract][Full Text] [Related]
4. Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.
Wei J; Xie Y; He W; Liu W; Jian W; Chen M; Wang D; Wang X; Sun X
Cytogenet Genome Res; 2014; 144(4):294-8. PubMed ID: 25634515
[TBL] [Abstract][Full Text] [Related]
5. Identification of iso(18p) marker chromosome by fluorescence in situ hybridization with single-copy DNA probe.
Nakashima H; Hasegawa T; Sakai M; Inaba R; Imamura T
Jpn J Hum Genet; 1995 Jun; 40(2):185-8. PubMed ID: 7662998
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. De novo isochromosome 18p in two patients: cytogenetic diagnosis and confirmation by chromosome painting.
Back E; Toder R; Voiculescu I; Wildberg A; Schempp W
Clin Genet; 1994 Jun; 45(6):301-4. PubMed ID: 7923860
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
[TBL] [Abstract][Full Text] [Related]
12. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
13. Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes.
Park VM; Gustashaw KM; Bilenker RM; Golden WL
Am J Med Genet; 1991 Nov; 41(2):180-3. PubMed ID: 1785630
[TBL] [Abstract][Full Text] [Related]
14. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
Zaki MS; Kamel AA; El-Ruby M
Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
[TBL] [Abstract][Full Text] [Related]
15. Two cases of Y; autosome translocations: A 45,X male and a clinically trisomy 18 patient.
Farah SB; Ramos CF; de Mello MP; Sartorato EL; Horelli-Kuitunen N; Lopes VL; Cavalcanti DP; Hackel C
Am J Med Genet; 1994 Feb; 49(4):388-92. PubMed ID: 8160730
[TBL] [Abstract][Full Text] [Related]
16. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
[TBL] [Abstract][Full Text] [Related]
17. Constitutional tetrasomy 18p.
Bakshi SR; Brahmbhatt MM; Trivedi PJ; Chudoba I
Indian Pediatr; 2006 Apr; 43(4):357-60. PubMed ID: 16651677
[TBL] [Abstract][Full Text] [Related]
18. [Case reports of patients with a marker chromosome].
Kocárek E; Novotná D; Maríková T; Cernáková I; Losan F; Balícek P; Baxová A; Havlovicová M; Goetz P
Cas Lek Cesk; 2004; 143(10):708-11; discussion 711-2. PubMed ID: 15584624
[TBL] [Abstract][Full Text] [Related]
19. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
Eur J Hum Genet; 2001 Aug; 9(8):572-6. PubMed ID: 11528501
[TBL] [Abstract][Full Text] [Related]
20. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
Brenk CH; Prott EC; Trost D; Hoischen A; Walldorf C; Radlwimmer B; Wieczorek D; Propping P; Gillessen-Kaesbach G; Weber RG; Engels H
Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
