BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 10399734)

  • 1. [Neurological aspects of two patients with non-mosaic and mosaic polysomy of the X and Y chromosomes].
    Jakubowski L; Sabatowska M; Filipiak-Miastkowska I; Nadratowski P; Rutkowska A; Nowakowska D; Kałuzewski B
    Neurol Neurochir Pol; 1999; 33(1):169-75. PubMed ID: 10399734
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 46,XY/47,XYY/48,XYYY karyotype in a 3-year-old boy ascertained because of radioulnar synostosis.
    James C; Robson L; Jackson J; Smith A
    Am J Med Genet; 1995 May; 56(4):389-92. PubMed ID: 7604847
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Mosaic 47,XY,+8/48,XXYY in a mentally non-retarded man with phenotypical and neurological abnormalities.
    Hoovers JM; Oorthuys JW; de Visser M
    Clin Genet; 1989 Jun; 35(6):446-9. PubMed ID: 2736792
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature].
    Donati F; Gasser S; Mullis P; Braga S; Vassella F
    Monatsschr Kinderheilkd; 1992 Apr; 140(4):216-9. PubMed ID: 1614446
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Radioulnar synostosis, behavioral disturbance, and XYY chromosomes.
    Cleveland WW; Arias D; Smith GF
    J Pediatr; 1969 Jan; 74(1):103-6. PubMed ID: 5782813
    [No Abstract]   [Full Text] [Related]  

  • 9. [Retardation of psychomotor development and tremor in a boy with 48,XXYY karyotype].
    Bayat M; Bayat A
    Ugeskr Laeger; 2014 Jan; 176(5A):V07130439. PubMed ID: 25347342
    [TBL] [Abstract][Full Text] [Related]  

  • 10. XXY male mice: an experimental model for Klinefelter syndrome.
    Lue Y; Rao PN; Sinha Hikim AP; Im M; Salameh WA; Yen PH; Wang C; Swerdloff RS
    Endocrinology; 2001 Apr; 142(4):1461-70. PubMed ID: 11250926
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Peculiar mosaicism 47,XYY/48,XYYY/49,XYYYY in man.
    Gigliani F; Gabellini P; Marcucci L; Petrinelli P; Antonelli A
    J Genet Hum; 1980 Mar; 28(1):47-51. PubMed ID: 7400784
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Epilepsy and tremor in the XXY syndrome].
    Roztoczyńska-Wodzień M; Róg T; Zwolińska G; Hubalewska-Hoła A; Czapiński P
    Neurol Neurochir Pol; 1992; 26(6):867-71. PubMed ID: 1301514
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. A male baboon (Papio hamadryas) with a mosaic 43,XXY/42,XY karyotype.
    Dudley CJ; Hubbard GB; Moore CM; Dunn BG; Raveendran M; Rogers J; Nathanielsz PW; McCarrey JR; Schlabritz-Loutsevitch NE
    Am J Med Genet A; 2006 Jan; 140(1):94-7. PubMed ID: 16315270
    [No Abstract]   [Full Text] [Related]  

  • 15. [Radioulnar synostosis as characteristic feature of chromosome aberrations (author's transl)].
    Küsswetter W; Heisel A
    Z Orthop Ihre Grenzgeb; 1981 Feb; 119(1):10-3. PubMed ID: 7281903
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ambiguous genitalia in an elderly woman with a mosaic 45,X/46,X,dic(Y)(Q11.2) karyotype.
    Smith YR; Stetten G; Charity L; Isacson C; Gearhart JP; Namnoum AB
    Urology; 1996 Feb; 47(2):259-62. PubMed ID: 8607249
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Klinefelter's syndrome, mosaic 46,XX/46,XY/47,XXY/48,XXXY/48,XXYY: a case report.
    Al-Awadi SA; Teebi AS; Krishna Murthy DS; Othman G; Sundareshan TS
    Ann Genet; 1986; 29(2):119-21. PubMed ID: 3490207
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of cryptic Y chromosome mosaicism by coamplification PCR with archived cytogenetic slides of suspected Turner syndrome.
    Kim JW; Cho EH; Kim YM; Kim JM; Han JY; Park SY
    Exp Mol Med; 2000 Mar; 32(1):38-41. PubMed ID: 10762060
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Y chromosome microdeletions in idiopathic azoospermia and non-mosaic type of Klinefelter syndrome.
    Lee YH; Kim T; Kim MH; Kim YT; Kim SH
    Exp Mol Med; 2000 Dec; 32(4):231-4. PubMed ID: 11190276
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.