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 *

199 related articles for article (PubMed ID: 6517096)

  • 1. Are the occasional aneuploid cells in peripheral blood cultures significant?
    Wenger SL; Golden WL; Dennis SP; Steele MW
    Am J Med Genet; 1984 Dec; 19(4):715-9. PubMed ID: 6517096
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytogenetic abnormalities in orthopedic patients.
    Cowell HR; Clark CE
    Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X chromosome aneuploidy in lymphocyte cultures from women with recurrent spontaneous abortions.
    Horsman DE; Dill FJ; McGillivray BC; Kalousek DK
    Am J Med Genet; 1987 Dec; 28(4):981-7. PubMed ID: 3688037
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaic status in lymphocytes of infertile men with or without Klinefelter syndrome.
    Lenz P; Luetjens CM; Kamischke A; Kühnert B; Kennerknecht I; Nieschlag E
    Hum Reprod; 2005 May; 20(5):1248-55. PubMed ID: 15665007
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Turner syndrome: a cytogenetic and molecular study.
    Jacobs P; Dalton P; James R; Mosse K; Power M; Robinson D; Skuse D
    Ann Hum Genet; 1997 Nov; 61(Pt 6):471-83. PubMed ID: 9543547
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Chromosomal factors in sterility in men].
    Ganev V
    Akush Ginekol (Sofiia); 1984; 23(1):88-93. PubMed ID: 6372537
    [No Abstract]   [Full Text] [Related]  

  • 8. A clinical and cytogenetic study of Turner syndrome.
    Suri M; Kabra M; Jain U; Sanders V; Saxena R; Shukla A; Singh GV; Verma IC
    Indian Pediatr; 1995 Apr; 32(4):433-42. PubMed ID: 8635807
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Kousseff BG; Diamond T; Essig Y; Miller K; Tedesco T
    Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
    Badalian LO; Mutovin GR; Malygina NA; Petrukhin AS
    Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex.
    Costa T; Lambert M; Teshima I; Ray PN; Richer CL; Dallaire L
    Am J Med Genet; 1998 Jan; 75(1):40-4. PubMed ID: 9450855
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Karyotype of amniotic fluid cells at the AUB-MC results on 2000 cases.
    Zahed L; al-Oreibi G; Darwiche N; el-Khechen S
    J Med Liban; 2000; 48(3):121-6. PubMed ID: 11268563
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
    Robson L; Jackson J; Cowell C; Sillence D; Smith A
    Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
    Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A; Blanco B; del Castillo V; Carnevale A
    Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and cytogenetic analyses in uveal melanoma.
    Kilic E; van Gils W; Lodder E; Beverloo HB; van Til ME; Mooy CM; Paridaens D; de Klein A; Luyten GP
    Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3703-7. PubMed ID: 16936076
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
    Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic studies of familial and sporadic Alzheimer disease.
    White BJ; Crandall C; Goudsmit J; Morrow CH; Alling DW; Gajdusek DC; Tijio JH
    Am J Med Genet; 1981; 10(1):77-89. PubMed ID: 7294063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular cytogenetic diagnosis of Klinefelter's syndrome in men more frequently detects sex chromosome mosaicism than classical cytogenetic methods].
    Kurková S; Zemanová Z; Hána V; Mayerová K; Pacovská K; Musilová J; Stĕpán J; Michalová K
    Cas Lek Cesk; 1999 Apr; 138(8):235-8. PubMed ID: 10510542
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.