269 related articles for article (PubMed ID: 1301994)
1. Rapid generation of region specific probes by chromosome microdissection and their application.
Meltzer PS; Guan XY; Burgess A; Trent JM
Nat Genet; 1992 Apr; 1(1):24-8. PubMed ID: 1301994
[TBL] [Abstract][Full Text] [Related]
2. Rapid generation of whole chromosome painting probes (WCPs) by chromosome microdissection.
Guan XY; Meltzer PS; Trent JM
Genomics; 1994 Jul; 22(1):101-7. PubMed ID: 7959755
[TBL] [Abstract][Full Text] [Related]
3. Metaphase FISH, microdissection, and multicolour FISH. Applications in haematology.
Mecucci C; Falzetti D; La Starza R
Haematologica; 1999 Jun; 84 Suppl EHA-4():98-101. PubMed ID: 10907483
[No Abstract] [Full Text] [Related]
4. Karyotyping human chromosomes by combinatorial multi-fluor FISH.
Speicher MR; Gwyn Ballard S; Ward DC
Nat Genet; 1996 Apr; 12(4):368-75. PubMed ID: 8630489
[TBL] [Abstract][Full Text] [Related]
5. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
Senger G; Chudoba I; Friedrich U; Tommerup N; Claussen U; Brøndum-Nielsen K
Prenat Diagn; 1997 Apr; 17(4):369-74. PubMed ID: 9160390
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. FISH of Alu-PCR-amplified YAC clones and applications in tumor cytogenetics.
Lengauer C; Speicher MR; Cremer T
Methods Mol Biol; 1994; 33():85-94. PubMed ID: 7894595
[No Abstract] [Full Text] [Related]
9. In situ hybridization of fluorescent probes on chromosomes, nuclei or stretched DNA: applications in physical mapping and characterization of genomic rearrangements.
Desmaze C; Aurias A
Cell Mol Biol (Noisy-le-grand); 1995 Nov; 41(7):925-31. PubMed ID: 8595371
[TBL] [Abstract][Full Text] [Related]
10. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P
Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
[TBL] [Abstract][Full Text] [Related]
11. Generation of FISH probes using laser microbeam microdissection and application to clinical molecular cytogenetics.
Shim SH; Kyhm JH; Chung SR; Kim SR; Park MI; Lee CH; Cho YH
J Microbiol Biotechnol; 2007 Jul; 17(7):1079-82. PubMed ID: 18051316
[TBL] [Abstract][Full Text] [Related]
12. Generation of alphoid DNA probes for fluorescence in situ hybridization (FISH) using the polymerase chain reaction.
Lengauer C; Dunham I; Featherstone T; Cremer T
Methods Mol Biol; 1994; 33():51-61. PubMed ID: 7894592
[No Abstract] [Full Text] [Related]
13. Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection.
Guan XY; Meltzer PS; Dalton WS; Trent JM
Nat Genet; 1994 Oct; 8(2):155-61. PubMed ID: 7842014
[TBL] [Abstract][Full Text] [Related]
14. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
[TBL] [Abstract][Full Text] [Related]
15. Fluorescent in situ hybridization as an adjunct to conventional cytogenetics.
Mark HF
Ann Clin Lab Sci; 1994; 24(2):153-63. PubMed ID: 8203823
[TBL] [Abstract][Full Text] [Related]
16. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of chromosome aberrations. In situ hybridization.
Lichter P; Ried T
Methods Mol Biol; 1994; 29():449-78. PubMed ID: 8032422
[No Abstract] [Full Text] [Related]
18. 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]
19. Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
Bryndorf T; Lundsteen C; Lamb A; Christensen B; Philip J
Acta Obstet Gynecol Scand; 2000 Jan; 79(1):8-14. PubMed ID: 10646809
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal cryptic insertion of the terminal region and its formative mechanism determined by fluorescence in situ hybridization.
Tan Y; Lu G
Chin Med J (Engl); 2002 Jul; 115(7):1039-42. PubMed ID: 12150739
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
