These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 12431259)

  • 1. Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences.
    Vermeesch JR; Baten E; Fryns JP; Devriendt K
    Clin Genet; 2002 Nov; 62(5):415-7. PubMed ID: 12431259
    [TBL] [Abstract][Full Text] [Related]  

  • 2. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
    Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
    Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability.
    Pezzolo A; Gimelli G; Cohen A; Lavaggetto A; Romano C; Fogu G; Zuffardi O
    Hum Genet; 1993 Aug; 92(1):23-7. PubMed ID: 8365723
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of mosaic ring chromosome 4 with subtelomeric 4p deletion].
    Kim JH; Oh PS; Na HY; Kim SH; Cho HC
    Korean J Lab Med; 2009 Feb; 29(1):77-81. PubMed ID: 19262083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ring chromosome 20 with loss of telomeric sequences detected by multicolour PRINS.
    Brandt CA; Kierkegaard O; Hindkjaer J; Jensen PK; Pedersen S; Therkelsen AJ
    Clin Genet; 1993 Jul; 44(1):26-31. PubMed ID: 8403451
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin.
    Miller K; Pabst B; Ritter H; Nürnberg P; Siebert R; Schmidtke J; Arslan-Kirchner M
    Hum Genet; 2003 Apr; 112(4):343-7. PubMed ID: 12574939
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.
    Elghezal H; Hannachi H; Mougou S; Kammoun H; Triki C; Saad A
    Eur J Med Genet; 2007; 50(6):441-5. PubMed ID: 17851150
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Delineation of a ring chromosome 16 by the FISH-technique: a case report with review.
    Conte RA; Kleyman SM; Kharode C; Verma RS
    Clin Genet; 1997 Mar; 51(3):196-9. PubMed ID: 9137886
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication of the Down syndrome critical region does not predict facial phenotype in a baby with a ring chromosome 21.
    Crombez EA; Dipple KM; Schimmenti LA; Rao N
    Clin Dysmorphol; 2005 Oct; 14(4):183-187. PubMed ID: 16155419
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Continuing role for classical cytogenetics: Case report of a boy with ring syndrome caused by complete ring chromosome 4 and review of literature.
    Burgemeister AL; Daumiller E; Dietze-Armana I; Klett C; Freiberg C; Stark W; Lingen M; Centonze I; Rettenberger G; Mehnert K; Zirn B
    Am J Med Genet A; 2017 Mar; 173(3):727-732. PubMed ID: 28127864
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ring chromosome 7 and sacral agenesis.
    Rodríguez L; Sanchís A; Villa A; Cánovas A; Peris S; Estívalis M; Pons S; Martínez-Frías ML
    Am J Med Genet; 2000 Sep; 94(1):52-8. PubMed ID: 10982483
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome.
    Sigurdardottir S; Goodman BK; Rutberg J; Thomas GH; Jabs EW; Geraghty MT
    Am J Med Genet; 1999 Dec; 87(5):384-90. PubMed ID: 10594875
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Supernumerary ring chromosome in a Bednar tumor (pigmented dermatofibrosarcoma protuberans) is composed of interspersed sequences from chromosomes 17 and 22: a fluorescence in situ hybridization and comparative genomic hybridization analysis.
    Nishio J; Iwasaki H; Ishiguro M; Ohjimi Y; Yo S; Isayama T; Naito M; Kikuchi M
    Genes Chromosomes Cancer; 2001 Mar; 30(3):305-9. PubMed ID: 11170290
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephaly.
    Sawyer JR; Lukacs JL; Hassed SJ; Arnold GL; Mitchell HF; Muenke M
    Am J Med Genet; 1996 Oct; 65(2):113-6. PubMed ID: 8911601
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14.
    Guilherme RS; de Freitas Ayres Meloni V; Sodré CP; Christofolini DM; Pellegrino R; de Mello CB; Conlin LK; Hutchinson AL; Spinner NB; Brunoni D; Kulikowski LD; Melaragno MI
    Am J Med Genet A; 2010 Nov; 152A(11):2865-9. PubMed ID: 20979193
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH.
    Dee SL; Clark AT; Willatt LR; Yates JR
    J Med Genet; 2001 Sep; 38(9):E32. PubMed ID: 11546833
    [No Abstract]   [Full Text] [Related]  

  • 19. Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome.
    Ricard-Mousnier B; N'Guyen S; Dubas F; Pouplard F; Guichet A
    Epileptic Disord; 2007 Sep; 9(3):327-31. PubMed ID: 17884758
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association.
    Kumar MJ; Kumar RA; Subhashree V; Jayasudha T; Hemagowri V; Koshy T; Gowrishankar K
    Cytogenet Genome Res; 2015; 146(2):120-123. PubMed ID: 26226839
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.