BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

412 related articles for article (PubMed ID: 8669444)

  • 1. Molecular studies of translocations and trisomy involving chromosome 13.
    Robinson WP; Bernasconi F; Dutly F; Lefort G; Romain DR; Binkert F; Schinzel AA
    Am J Med Genet; 1996 Jan; 61(2):158-63. PubMed ID: 8669444
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parental origin determination in thirty de novo Robertsonian translocations.
    Shaffer LG; Jackson-Cook CK; Stasiowski BA; Spence JE; Brown JA
    Am J Med Genet; 1992 Aug; 43(6):957-63. PubMed ID: 1357969
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically.
    Blouin JL; Binkert F; Antonarakis SE
    Am J Med Genet; 1994 Feb; 49(3):363-8. PubMed ID: 8209906
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.
    Berend SA; Feldman GL; McCaskill C; Czarnecki P; Van Dyke DL; Shaffer LG
    Am J Med Genet; 1999 Jan; 82(3):275-81. PubMed ID: 10215554
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
    Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2010 Mar; 49(1):62-8. PubMed ID: 20466295
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
    Mau UA; Petruch UR; Kaiser P; Eggermann T
    Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-disjunction of chromosome 13.
    Bugge M; Collins A; Hertz JM; Eiberg H; Lundsteen C; Brandt CA; Bak M; Hansen C; Delozier CD; Lespinasse J; Tranebjaerg L; Hahnemann JM; Rasmussen K; Bruun-Petersen G; Duprez L; Tommerup N; Petersen MB
    Hum Mol Genet; 2007 Aug; 16(16):2004-10. PubMed ID: 17584770
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosis.
    Soler A; Margarit E; Queralt R; Carrió A; Costa D; Gómez D; Ballesta F
    Am J Med Genet; 2000 Feb; 90(4):291-3. PubMed ID: 10710225
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.
    Silverstein S; Lerer I; Sagi M; Frumkin A; Ben-Neriah Z; Abeliovich D
    Prenat Diagn; 2002 Aug; 22(8):649-51. PubMed ID: 12210570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B; Kotzot D; Brecevic L; Koehler M; Balmer D; Binkert F; Schinzel A
    Eur J Hum Genet; 1999 Dec; 7(8):873-83. PubMed ID: 10602362
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A somatic origin of homologous Robertsonian translocations and isochromosomes.
    Robinson WP; Bernasconi F; Basaran S; Yüksel-Apak M; Neri G; Serville F; Balicek P; Haluza R; Farah LM; Lüleci G
    Am J Hum Genet; 1994 Feb; 54(2):290-302. PubMed ID: 8304346
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.
    Ruggeri A; Dulcetti F; Miozzo M; Grati FR; Grimi B; Bellato S; Natacci F; Maggi F; Simoni G
    Prenat Diagn; 2004 Dec; 24(12):997-1000. PubMed ID: 15614836
    [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. Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment.
    Robinson WP; Bernasconi F; Lau A; McFadden DE
    Am J Med Genet; 1999 May; 84(1):34-42. PubMed ID: 10213044
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cytogenetic and age-dependent risk factors associated with uniparental disomy 15.
    Robinson WP; Langlois S; Schuffenhauer S; Horsthemke B; Michaelis RC; Christian S; Ledbetter DH; Schinzel A
    Prenat Diagn; 1996 Sep; 16(9):837-44. PubMed ID: 8905898
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
    Daniel A; Hook EB; Wulf G
    Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocation.
    Van den Boogaard MJ; De Pater J; Hennekam RC
    Genet Couns; 1991; 2(2):83-91. PubMed ID: 1781959
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.