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 *

1161 related articles for article (PubMed ID: 16900777)

  • 1. 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]  

  • 2. Forty-two supernumerary marker chromosomes (SMCs) in 43,273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies.
    Bartsch O; Loitzsch A; Kozlowski P; Mazauric ML; Hickmann G
    Eur J Hum Genet; 2005 Nov; 13(11):1192-204. PubMed ID: 16077735
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
    Huang B; Solomon S; Thangavelu M; Peters K; Bhatt S
    Prenat Diagn; 2006 Dec; 26(12):1142-50. PubMed ID: 17009345
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
    Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature.
    Crolla JA
    Am J Med Genet; 1998 Feb; 75(4):367-81. PubMed ID: 9482642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O; Rasi S; Hoffmann K; Blin N
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited.
    Crolla JA; Youings SA; Ennis S; Jacobs PA
    Eur J Hum Genet; 2005 Feb; 13(2):154-60. PubMed ID: 15508017
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
    Rowe AG; Abrams L; Qu Y; Chen E; Cotter PD
    Am J Med Genet; 2000 Aug; 93(5):393-8. PubMed ID: 10951463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15.
    Cotter PD; Ledesma CT; Dietz LG; Pusso S; Wohlferd MM; Goldberg JD
    Prenat Diagn; 1999 Aug; 19(8):721-6. PubMed ID: 10451515
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
    Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
    Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 59.