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 *

355 related articles for article (PubMed ID: 7091197)

  • 1. Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.
    Stine SB; Clark CE; Telfer MA; Casey PA; Cowell HR
    Am J Med Genet; 1982 May; 12(1):57-62. PubMed ID: 7091197
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X microchromosome with additional chromosome anomalies found in Ullrich-Turner syndrome.
    Wydner KL; Li M; Singer-Granick C; Sciorra LJ; Krueger LJ
    Am J Med Genet; 1995 Mar; 56(2):141-6. PubMed ID: 7625435
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Pericentric inversions of chromosomes 1, 9 and 16 in patients with sex chromosome anomalies].
    Verlinskaia DK; Prozorova MV; Khitrikov LE
    Tsitol Genet; 1982; 16(1):57-60. PubMed ID: 7064223
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    Canún S; Mutchinick O; Shaffer LG; Fernández C
    Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome.
    Grompe M; Rao N; Elder FF; Caskey CT; Greenberg F
    Am J Med Genet; 1992 Jan; 42(1):39-43. PubMed ID: 1339199
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome.
    Burégio-Frota P; Valença L; Leal GF; Duarte AR; Bispo-Brito AV; Soares-Ventura EM; Marques-Salles TJ; Nogueira MT; Muniz MT; Silva ML; Hunstig F; Liehr T; Santos N
    Genet Mol Res; 2010 Apr; 9(2):780-4. PubMed ID: 20449811
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv(2) (p15 q21)] in a patient with gonadal dysgenesis.
    Cohen MM; Rosenmann A; Hacham-Zadeh S; Dahan S
    Clin Genet; 1975 Jul; 8(1):11-7. PubMed ID: 1149316
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.
    Kleczkowska A; Dmoch E; Kubien E; Fryns JP; Van den Berghe H
    Genet Couns; 1990; 1(3-4):227-33. PubMed ID: 2098046
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Longitudinal differentiation of human mitotic chromosomes. Communication II. Analysis of pericentric inversion of the first chromosome in a child with anomalous sex differentiation.
    Seleznev YuV ; Dzenis IG
    Sov Genet; 1974 Jul; 8(6):770-3. PubMed ID: 4421586
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. [Pericentric inversion of chromosome 7 associated with 45,X Turner syndrome ].
    Carnevale A; Mayén DG; Blanco B
    Rev Invest Clin; 1986; 38(4):425-8. PubMed ID: 3563146
    [No Abstract]   [Full Text] [Related]  

  • 13. [Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st report].
    Vignetti P; Brinchi V; Bruni L; Rizzuti A; Tarani L; Tozzi MC
    Minerva Pediatr; 1990; 42(1-2):25-7. PubMed ID: 2336052
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
    Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recombinant chromosome as a result of pericentric inversion of X chromosome.
    Nikolis J; Stolević E
    Hum Genet; 1978 Dec; 45(2):115-22. PubMed ID: 738716
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Rare chromosomal aberrations in the Shereshevskiĭ-Turner syndrome].
    Shandlorenko SK; Maksimova SP; Verlinskaia DK
    Tsitologiia; 1986 Jul; 28(7):748-50. PubMed ID: 3765110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Turner's syndrome and a probable pericentric inversion of chromosome 2(45, X, 2(p+q-))].
    Hooft C; Coetsier H; Orye E
    Ann Genet; 1968 Sep; 11(3):181-3. PubMed ID: 5304738
    [No Abstract]   [Full Text] [Related]  

  • 18. [Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]].
    Baumann W; Zabel B; Holl M
    Ann Genet; 1984; 27(2):106-8. PubMed ID: 6331785
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
    Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
    Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 18.