158 related articles for article (PubMed ID: 2709396)
1. Identification and characterisation of a small marker chromosome using non-isotopic in situ hybridisation with X and Y specific probes.
Crolla JA; Smith M; Docherty Z
J Med Genet; 1989 Mar; 26(3):192-4. PubMed ID: 2709396
[TBL] [Abstract][Full Text] [Related]
2. An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes.
Cooper C; Crolla JA; Laister C; Johnston DI; Cooke P
J Med Genet; 1991 Jan; 28(1):6-9. PubMed ID: 1999837
[TBL] [Abstract][Full Text] [Related]
3. A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique.
Crolla JA; Llerena JC
Hum Genet; 1988 Dec; 81(1):81-4. PubMed ID: 3198130
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
Wolff DJ; Brown CJ; Schwartz S; Duncan AM; Surti U; Willard HF
Am J Hum Genet; 1994 Jul; 55(1):87-95. PubMed ID: 8023855
[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. Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies.
Petrovic V; Nasioulas S; Chow CW; Voullaire L; Schmidt M; Dahl H
J Med Genet; 1992 Aug; 29(8):542-6. PubMed ID: 1518023
[TBL] [Abstract][Full Text] [Related]
8. A small supernumerary marker chromosome X identified by in situ hybridization.
Silahtaroglu AN; Hacihanefioglu S; Yilmaz S; Tarkan Y; Cenani A; Tümer Z
Clin Genet; 1995 May; 47(5):270-3. PubMed ID: 7554355
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Elucidation of structural abnormalities of the X chromosome using fluorescence in situ hybridisation with a Y chromosome painting probe.
Howell RT; Millener R; Thorne S; O'Loughlin J; Brassey J; McDermott A
J Med Genet; 1994 Mar; 31(3):206-8. PubMed ID: 8014968
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Detection of t(X;Y) in 2 XX males using fluorescent in situ hybridization.
Taiar N; Qumsiyeh MB; Croteau S; Rollet J; Benkhalifa M
Ann Genet; 1995; 38(2):102-5. PubMed ID: 7486824
[TBL] [Abstract][Full Text] [Related]
13. Relevance to prenatal diagnosis of the identification of a human Y/autosome translocation by Y-chromosome-specific in situ hybridisation.
Ellis PM; West JD; West KM; Murray RS; Coyle MC
Mol Reprod Dev; 1990 Jan; 25(1):37-41. PubMed ID: 2393582
[TBL] [Abstract][Full Text] [Related]
14. A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.
Crolla JA; Dennis NR; Jacobs PA
J Med Genet; 1992 Oct; 29(10):699-703. PubMed ID: 1433228
[TBL] [Abstract][Full Text] [Related]
15. A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308.
Callen DF; Eyre HJ; Ringenbergs ML
Clin Genet; 1990 Feb; 37(2):81-3. PubMed ID: 2311270
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.
Callen DF; Eyre HJ; Dolman G; Garry-Battersby MB; McCreanor JR; Valeba A; McGill JJ
J Med Genet; 1995 Feb; 32(2):113-6. PubMed ID: 7760319
[TBL] [Abstract][Full Text] [Related]
17. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
Robson L; Jackson J; Cowell C; Sillence D; Smith A
Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669
[TBL] [Abstract][Full Text] [Related]
18. Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y-chromosome marker, idic(Yp).
Bernstein R; Steinhaus KA; Cain MJ
Prenat Diagn; 1992 Sep; 12(9):709-16. PubMed ID: 1438065
[TBL] [Abstract][Full Text] [Related]
19. Duplication of the short arm of the X chromosome in mother and daughter.
Tuck-Muller CM; Martinez JE; Batista DA; Kearns WG; Wertelecki W
Hum Genet; 1993 May; 91(4):395-400. PubMed ID: 8500796
[TBL] [Abstract][Full Text] [Related]
20. Ring Y chromosome: molecular characterization by DNA probes.
Pohlschmidt M; Rappold G; Krause M; Ahlert D; Hosenfeld D; Weissenbach J; Gal A
Cytogenet Cell Genet; 1991; 56(2):65-8. PubMed ID: 2013232
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
