BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

302 related articles for article (PubMed ID: 16531734)

  • 21. [Trisomy 4p as result of a maternal translocation t(4;8)(q11;p23)].
    Stumm M; Reuter M; Mandon U; Brückner R; Wieacker P
    Klin Padiatr; 1999; 211(1):35-9. PubMed ID: 10067217
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)].
    Andrle M; Erlach A; Rett A
    Wien Klin Wochenschr; 1981 Jan; 93(1):16-9. PubMed ID: 7222705
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.
    Petit P; Fryns JP
    Genet Couns; 1990; 1(2):179-84. PubMed ID: 2081002
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.
    Azman BZ; Akhir SM; Zilfalil BA; Ankathil R
    Singapore Med J; 2008 Apr; 49(4):e98-e100. PubMed ID: 18418516
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J; Chernos J; Roland B
    Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature review.
    Frints SG; Schrander-Stumpel CT; Engelen JJ; Da Costa AJ; Fryns JP
    Genet Couns; 1996; 7(2):135-42. PubMed ID: 8831133
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Family with partial monosomy 10p and trisomy 10p.
    Hon E; Chapman C; Gunn TR
    Am J Med Genet; 1995 Mar; 56(2):136-40. PubMed ID: 7625434
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
    Chen CP; Lin CC; Chang TY; Li YC; Hsieh LJ; Lee CC; Chen LF; Wang W
    Prenat Diagn; 2006 Aug; 26(8):757-9. PubMed ID: 16865745
    [No Abstract]   [Full Text] [Related]  

  • 31. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D; Boccone L; Ristaldi MS; Nucaro AL
    Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literature.
    Iqbal MA; Ahmed MZ; Wu D; Sakati N
    Am J Med Genet; 1997 May; 70(2):174-8. PubMed ID: 9128939
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA; Legat G; Trautmann U
    Ann Genet; 1992; 35(1):41-6. PubMed ID: 1610119
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes.
    Byatt SA; Baker E; Richards RI; Roberts C; Smith A
    Am J Med Genet; 1997 Jun; 70(4):357-60. PubMed ID: 9182774
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Intracytoplasmic sperm injection pregnancy with trisomy 20p and monosomy 22q in a newborn resulting from a balanced paternal translocation.
    Belin V; Farhat M; Monset-Couchard M
    Biol Neonate; 1999; 75(6):398-401. PubMed ID: 10325443
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
    Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
    Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy].
    Xiao W; Gao Z; Meng Q; Zhang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):747-9. PubMed ID: 25449080
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fishing for a diagnosis.
    Duijvestijn YC; Cobben JM; Leegte B; de Vries TW
    Genet Couns; 2002; 13(1):49-54. PubMed ID: 12017238
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C; Crippa L; Delozier C; Michail E; Graber P
    J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.