182 related articles for article (PubMed ID: 8766134)
1. 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]
2. 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]
3. The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.
Karaman B; Aytan M; Yilmaz K; Toksoy G; Onal EP; Ghanbari A; Engur A; Kayserili H; Yuksel-Apak M; Basaran S
Eur J Med Genet; 2006; 49(3):207-14. PubMed ID: 16762822
[TBL] [Abstract][Full Text] [Related]
4. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.
Li MM; Howard-Peebles PN; Killos LD; Fallon L; Listgarten E; Stanley WS
Prenat Diagn; 2000 Feb; 20(2):138-43. PubMed ID: 10694686
[TBL] [Abstract][Full Text] [Related]
5. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.
van den Berg C; Pijpers L; Halley DJ; Opstal DV; Los FJ
Am J Med Genet; 1999 Sep; 86(2):151-5. PubMed ID: 10449651
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
Graf MD; Gill P; Krew M; Schwartz S
Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
[TBL] [Abstract][Full Text] [Related]
8. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
Mechoso B; Vaglio A; Quadrelli A; Mark HF; Huang XL; Milunsky A; Quadrelli R
Fetal Diagn Ther; 2007; 22(4):249-53. PubMed ID: 17369689
[TBL] [Abstract][Full Text] [Related]
9. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
Wang H; Li H; Wang H; Wang H; Xia Y; Wen J; Long Z; Dai H; Liang D; Xia J; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
[TBL] [Abstract][Full Text] [Related]
10. [Cytogenic characterization of chromosome markers detected at amniocentesis: implications for karyotype-phenotype correlations].
Valerio D; Aiello R; Altieri V; Antonucci F
Minerva Ginecol; 1996 Sep; 48(9):365-9. PubMed ID: 8999384
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.
Pierluigi M; Battaglia P; Perfumo C; Baroncini A; Bricarelli FD
Ann Genet; 1997; 40(2):99-103. PubMed ID: 9259956
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Prenatal diagnosis of tetrasomy 18p using multiplex fluorescent PCR and comparison with a variety of techniques.
Irwin DL; Bryan JL; Chan FY; Matthews PL; Healey SC; Peters M; Findlay I
Genet Test; 2003; 7(1):1-6. PubMed ID: 12820695
[TBL] [Abstract][Full Text] [Related]
16. Characterisation of supernumerary chromosomal markers: a study of 13 cases.
Douet-Guilbert N; Marical H; Pinson L; Herry A; Le Bris MJ; Morel F; De Braekeleer M
Cytogenet Genome Res; 2007; 116(1-2):18-23. PubMed ID: 17268173
[TBL] [Abstract][Full Text] [Related]
17. Post-zygotic origin of isochromosome 12p.
de Ravel TJ; Keymolen K; van Assche E; Wittevronghel I; Moerman P; Salden I; Matthijs G; Fryns JP; Vermeesch JR
Prenat Diagn; 2004 Dec; 24(12):984-8. PubMed ID: 15614858
[TBL] [Abstract][Full Text] [Related]
18. Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.
Polityko AD; Goncharova E; Shamgina L; Drozdovskaja N; Podleschuk L; Abramchik E; Jaroshevich E; Khurs O; Pisarik I; Pribushenya O; Rumyantseva N; Naumchik I
J Histochem Cytochem; 2005 Mar; 53(3):361-4. PubMed ID: 15750020
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping.
Ning Y; Laundon CH; Schröck E; Buchanan P; Ried T
Prenat Diagn; 1999 May; 19(5):480-2. PubMed ID: 10360520
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome.
Yakut S; Sanhal C; Manguoglu E; Cetin Z
Genet Couns; 2014; 25(3):257-64. PubMed ID: 25365847
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
