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 *

129 related articles for article (PubMed ID: 433925)

  • 21. Cytogenetic studies in a population suspected to have chromosomal abnormalities.
    Shah VC; Murthy DS; Murthy SK
    Indian J Pediatr; 1990; 57(2):235-43. PubMed ID: 2246022
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
    López-Pajares I; Martin-Ancel A; Cabello P; Delicado A; Garcia-Alix A; San Roman C
    Clin Genet; 1993 Feb; 43(2):94-7. PubMed ID: 8448910
    [TBL] [Abstract][Full Text] [Related]  

  • 23. First trimester chromosomal analysis of complex structural rearrangements with RHA banding on chorionic villi.
    Sachs ES; Van Hemel JO; Galjaard H; Niermeijer MF; Jahoda MG
    Lancet; 1983 Dec; 2(8364):1426. PubMed ID: 6140529
    [No Abstract]   [Full Text] [Related]  

  • 24. Clinical significance of the satellited short arm of human chromosome 17 (17ps +) : a rare heteromorphism?
    Verma RS; Ved Brat S; Warman J; Dosik H
    Ann Genet; 1979; 22(3):133-6. PubMed ID: 316666
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Routine cytogenetic prenatal diagnosis using dynamic banding (RBG-GBG): a highly reproducible method for amniocytes, fetal cord blood, and chorionic villus investigations.
    Savary JB; Vasseur F; Lai JL; Daudignon A; Deminatti M
    Prenat Diagn; 1991 Dec; 11(12):883-91. PubMed ID: 1805195
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
    Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
    Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chromosome banding and identification. Fluorescence.
    Sumner AT
    Methods Mol Biol; 1994; 29():83-96. PubMed ID: 7518288
    [No Abstract]   [Full Text] [Related]  

  • 28. [Diagnostic advances in chromosomal analysis].
    Ballesta Martínez F
    An Esp Pediatr; 1991 Dec; 35 Suppl 47():106-10. PubMed ID: 1821556
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Determination of the breakpoints and the parental origin of a ring 22 chromosome: an analysis by high-resolution banding technique, quinacrine and silver stainings.
    Naritomi K; Hirayama K
    Jinrui Idengaku Zasshi; 1988 Mar; 33(1):67-73. PubMed ID: 2455825
    [No Abstract]   [Full Text] [Related]  

  • 30. Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.
    Weise A; Starke H; Heller A; Tönnies H; Volleth M; Stumm M; Gabriele S; Nietzel A; Claussen U; Liehr T
    J Med Genet; 2002 Jun; 39(6):434-9. PubMed ID: 12070255
    [No Abstract]   [Full Text] [Related]  

  • 31. [Indications for chromosomal analysis].
    Sakamoto H
    Rinsho Byori; 1989 Feb; Spec No 80():12-20. PubMed ID: 2630660
    [No Abstract]   [Full Text] [Related]  

  • 32. Application of multicolor banding for identification of complex chromosome 18 rearrangements.
    Hu J; Sathanoori M; Kochmar SJ; Surti U
    J Mol Diagn; 2006 Sep; 8(4):521-5; quiz 528. PubMed ID: 16931594
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [The clinical application of spectral karyotyping in the analysis of chromosomal abnormalities].
    Guo QS; Zhang YP; Li XT; Han JL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):80-3. PubMed ID: 17285551
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [New applications of cytogenetics in the diagnosis of congenital defects].
    Dallapiccola B
    Pathologica; 1986; 78(1058):709-29. PubMed ID: 3320906
    [No Abstract]   [Full Text] [Related]  

  • 35. The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.
    Ohta T; Tohma T; Soejima H; Fukushima Y; Nagai T; Yoshiura K; Jinno Y; Niikawa N
    Hum Genet; 1993 Aug; 92(1):1-5. PubMed ID: 8365720
    [TBL] [Abstract][Full Text] [Related]  

  • 36. mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations.
    Chudoba I; Hickmann G; Friedrich T; Jauch A; Kozlowski P; Senger G
    Cytogenet Genome Res; 2004; 104(1-4):390-3. PubMed ID: 15162070
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 18ph+ is a normal chromosomal variant.
    Hoo JJ; Robertson A
    Clin Genet; 1987 Jul; 32(1):79-80. PubMed ID: 3621658
    [No Abstract]   [Full Text] [Related]  

  • 38. [Autosomal chromosome aberrations].
    Schinzel A
    Ther Umsch; 1986 Dec; 43(12):882-7. PubMed ID: 3824258
    [No Abstract]   [Full Text] [Related]  

  • 39. Improved definition of chromosomal breakpoints using high-resolution multicolour banding.
    Lemke J; Chudoba I; Senger G; Stumm M; Loncarevic IF; Henry C; Zabel B; Claussen U
    Hum Genet; 2001 Jun; 108(6):478-83. PubMed ID: 11499672
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The usefulness of chromosome banding in pre- and postnatal service cytogenetics: a reconsideration.
    Feeny D; Tomkins DJ
    Am J Med Genet; 1981; 9(1):79-85. PubMed ID: 6787921
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.