BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

435 related articles for article (PubMed ID: 8322813)

  • 21. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.
    Krasikov N; Takaesu N; Hassold T; Knops JF; Finley WH; Scarbrough P
    Am J Med Genet; 1992 Jun; 43(3):554-60. PubMed ID: 1605248
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.
    Fryns JP; Kleczkowska A; Decock P; Van den Berghe H
    Ann Genet; 1990; 33(1):46-8. PubMed ID: 2195981
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G; Decock P; Fryns JP
    Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
    Tonnies H; Gerlach A; Heineking B; Starke H; Neitzel H; Neumann LM
    Cytogenet Genome Res; 2006; 114(3-4):325-9. PubMed ID: 16954674
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 27. De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.
    Dufke A; Singer S; Borell-Kost S; Stotter M; Pflumm DA; Mau-Holzmann UA; Starke H; Mrasek K; Enders H
    Cytogenet Genome Res; 2006; 114(3-4):342-50. PubMed ID: 16954677
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.
    Lindsay EA; Shaffer LG; Carrozzo R; Greenberg F; Baldini A
    Am J Med Genet; 1995 Apr; 56(3):296-9. PubMed ID: 7778594
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
    Barber JC; James RS; Patch C; Temple IK
    Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A paternally derived inverted duplication of 7q with evidence of a telomeric deletion.
    Stetten G; Charity LL; Kasch LM; Scott AF; Berman CL; Pressman E; Blakemore KJ
    Am J Med Genet; 1997 Jan; 68(1):76-81. PubMed ID: 8986281
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
    Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
    Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe.
    Meguid NA; Habibian R
    Clin Genet; 1992 May; 41(5):225-8. PubMed ID: 1606710
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome].
    Han X; Zhang JM; Jiang WT; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):361-6. PubMed ID: 20677137
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Confirmation of proximal 1q duplication using fluorescence in situ hybridization.
    Chen H; Kusyk CJ; Tuck-Muller CM; Martinez JE; Dorand RD; Wertelecki W
    Am J Med Genet; 1994 Mar; 50(1):28-31. PubMed ID: 8160749
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathy.
    Witters I; Van Buggenhout G; Moerman P; Fryns JP
    Prenat Diagn; 1998 Dec; 18(12):1304-7. PubMed ID: 9885024
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
    Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
    Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
    Lindgren V; Rosinsky B; Chin J; Berry-Kravis E
    Am J Med Genet; 1994 Jan; 49(1):67-73. PubMed ID: 8172253
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V; Fernandez-Novoa C; Hevia A; Novales A; Fornell J; Galera H
    Ann Genet; 1981; 24(4):248-50. PubMed ID: 6977308
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A large kindred with an INV(3)(p25q23): clinical, cytogenetic and genetic marker studies.
    Sutherland GR; Mulley JC; Goldblatt E
    Ann Genet; 1981; 24(4):202-5. PubMed ID: 6977298
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 22.