BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 20034065)

  • 1. A paternally transmitted complex chromosomal rearrangement (CCR) involving chromosomes 2, 6, and 18 includes eight breakpoints and five insertional translocations (ITs) through three generations.
    Gruchy N; Barreau M; Kessler K; Gourdier D; Leporrier N
    Am J Med Genet A; 2010 Jan; 152A(1):185-90. PubMed ID: 20034065
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR):  Molecular Cytogenetic Analysis.
    Olszewska M; Stokowy T; Pollock N; Huleyuk N; Georgiadis A; Yatsenko S; Zastavna D; Yatsenko AN; Kurpisz M
    Int J Mol Sci; 2020 Jun; 21(12):. PubMed ID: 32604929
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
    Kontodiou M; Daskalakis G; Vetro A; Paspaliaris V; Papaioannou G; Dagklis T; Tsakiridis I; Ziegler M; Liehr T; Thomaidis L; Papoulidis I; Manolakos E
    Cytogenet Genome Res; 2015; 147(2-3):118-23. PubMed ID: 26681178
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review.
    Batanian JR; Eswara MS
    Am J Med Genet; 1998 Jun; 78(1):44-51. PubMed ID: 9637422
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.
    Horn D; Neitzel H; Tönnies H; Kalscheuer V; Kunze J; Hinkel GK; Bartsch O
    Am J Med Genet A; 2003 Mar; 117A(3):236-44. PubMed ID: 12599186
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Unstable transmission of a familial complex chromosome rearrangement.
    van Binsbergen E; Hochstenbach R; Giltay J; Swinkels M
    Am J Med Genet A; 2012 Nov; 158A(11):2888-93. PubMed ID: 22987625
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
    Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
    Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
    Berend SA; Bodamer OA; Shapira SK; Shaffer LG; Bacino CA
    Am J Med Genet; 2002 May; 109(4):311-7. PubMed ID: 11992486
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report.
    Joly-Helas G; de La Rochebrochard C; Mousset-Siméon N; Moirot H; Tiercin C; Romana SP; Le Caignec C; Clavier B; Macé B; Rives N
    Hum Reprod; 2007 May; 22(5):1292-7. PubMed ID: 17283038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints.
    Lee NC; Chen M; Ma GC; Lee DJ; Wang TJ; Ke YY; Chien YH; Hwu WL
    Am J Med Genet A; 2010 Sep; 152A(9):2327-34. PubMed ID: 20684005
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
    Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA; Pai GS; Stetten G
    Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14', 15, and 21 leading to balanced and unbalanced rearrangements in offspring.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Margarit E; Borrell A
    Am J Med Genet A; 2005 Apr; 134(3):309-14. PubMed ID: 15732062
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
    Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
    Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.
    Trpchevska N; Dimova I; Arabadji T; Milachich T; Angelova S; Dimitrova M; Hristova-Savova M; Andreeva P; Timeva T; Shterev A
    J Assist Reprod Genet; 2017 May; 34(5):659-669. PubMed ID: 28236108
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
    Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T
    Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exceptional complex chromosomal rearrangements in three generations.
    Kartapradja H; Marzuki NS; Pertile MD; Francis D; Suciati LP; Anggaratri HW; Ambarwati DD; Idris FP; Lesmana H; Trimarsanto H; Paramayuda C; Harahap AR
    Case Rep Genet; 2015; 2015():321014. PubMed ID: 25722897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of a balanced complex chromosomal rearrangement carrier ascertained through a fetus with dup15q26.3 and del5p15.33: case report.
    Lledo B; Ortiz JA; Morales R; Manchon I; Galan F; Bernabeu A; Bernabeu R
    Hum Fertil (Camb); 2013 Sep; 16(3):215-7. PubMed ID: 23905868
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.