109 related articles for article (PubMed ID: 8782825)
1. A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration.
Nat Genet; 1996 Sep; 14(1):86-9. PubMed ID: 8782825
[TBL] [Abstract][Full Text] [Related]
2. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
Bacino CA; Kashork CD; Davino NA; Shaffer LG
Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
[TBL] [Abstract][Full Text] [Related]
3. Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.
Joyce CA; Dennis NR; Cooper S; Browne CE
Hum Genet; 2001 Oct; 109(4):440-51. PubMed ID: 11702226
[TBL] [Abstract][Full Text] [Related]
4. Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies.
Wakui K; Tanemura M; Suzumori K; Hidaka E; Ishikawa M; Kubota T; Fukushima Y
J Hum Genet; 1999; 44(2):85-90. PubMed ID: 10083730
[TBL] [Abstract][Full Text] [Related]
5. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
6. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
Ballif BC; Kashork CD; Shaffer LG
Eur J Hum Genet; 2000 Oct; 8(10):764-70. PubMed ID: 11039576
[TBL] [Abstract][Full Text] [Related]
7. Cryptic telomere imbalance: a 15-year update.
Ledbetter DH; Martin CL
Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):327-34. PubMed ID: 17910073
[TBL] [Abstract][Full Text] [Related]
8. Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.
Sismani C; Armour JA; Flint J; Girgalli C; Regan R; Patsalis PC
Eur J Hum Genet; 2001 Jul; 9(7):527-32. PubMed ID: 11464244
[TBL] [Abstract][Full Text] [Related]
9. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
[TBL] [Abstract][Full Text] [Related]
10. Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities.
Fortin F; Beaulieu Bergeron M; Fetni R; Lemieux N
Cytogenet Genome Res; 2009; 125(3):176-85. PubMed ID: 19738378
[TBL] [Abstract][Full Text] [Related]
11. Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short arms.
Sutton VR; Coveler KJ; Lalani SR; Kashork CD; Shaffer LG
Am J Med Genet; 2002 Sep; 112(1):23-7. PubMed ID: 12239715
[TBL] [Abstract][Full Text] [Related]
12. Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.
Tosi S; Giudici G; Rambaldi A; Scherer SW; Bray-Ward P; Dirscherl L; Biondi A; Kearney L
Genes Chromosomes Cancer; 1999 Mar; 24(3):213-21. PubMed ID: 10451701
[TBL] [Abstract][Full Text] [Related]
13. Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.
Engels H; Ehrbrecht A; Zahn S; Bosse K; Vrolijk H; White S; Kalscheuer V; Hoovers JM; Schwanitz G; Propping P; Tanke HJ; Wiegant J; Raap AK
Eur J Hum Genet; 2003 Sep; 11(9):643-51. PubMed ID: 12939649
[TBL] [Abstract][Full Text] [Related]
14. Evaluation of MLPA for the detection of cryptic subtelomeric rearrangements.
Monfort S; Orellana C; Oltra S; Roselló M; Guitart M; Martínez F
J Lab Clin Med; 2006 Jun; 147(6):295-300. PubMed ID: 16750667
[TBL] [Abstract][Full Text] [Related]
15. Double telomeric signals on single chromatids revealed by FISH and PRINS.
Philippe C; Coullin P; Bernheim A
Ann Genet; 1999; 42(4):202-9. PubMed ID: 10674159
[TBL] [Abstract][Full Text] [Related]
16. Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres.
Knight SJ; Horsley SW; Regan R; Lawrie NM; Maher EJ; Cardy DL; Flint J; Kearney L
Eur J Hum Genet; 1997; 5(1):1-8. PubMed ID: 9156314
[TBL] [Abstract][Full Text] [Related]
17. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
Boehm D; Herold S; Kuechler A; Liehr T; Laccone F
Hum Mutat; 2004 Apr; 23(4):368-78. PubMed ID: 15024731
[TBL] [Abstract][Full Text] [Related]
18. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
[TBL] [Abstract][Full Text] [Related]
19. Subtelomeric rearrangements: results from FISH studies in 84 families with idiopathic mental retardation.
Bocian E; Hélias-Rodzewicz Z; Suchenek K; Obersztyn E; Kutkowska-Kaźmierczak A; Stankiewicz P; Kostyk E; Mazurczak T
Med Sci Monit; 2004 Apr; 10(4):CR143-51. PubMed ID: 15039644
[TBL] [Abstract][Full Text] [Related]
20. Fluorescence in situ hybridization (FISH) in cytogenetics of leukemia.
Michalová K
Folia Biol (Praha); 1996; 42(6):311-4. PubMed ID: 9158941
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
