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 *

368 related articles for article (PubMed ID: 8042669)

  • 1. 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]  

  • 2. [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]  

  • 3. 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]  

  • 4. An atypical Turner syndrome patient with ring X chromosome mosaicism.
    Cantú ES; Jacobs DF; Pai GS
    Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytogenetic evaluation, fluorescence in situ hybridization, and molecular study of psu idic(X)(pter-->q22.3::q22.3-->pter) chromosome abberation in a girl with moderate growth retardation.
    Petković I; Barisić I; Bago R
    Croat Med J; 2003 Aug; 44(4):494-9. PubMed ID: 12950157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. FISH techniques in a Turner mosaic with ring X chromosome.
    Rajangam S; Lincoln S; Hegde S; Jayashree ; Manjunath NA; Thomas IM
    Indian Pediatr; 1993 Dec; 30(12):1451-4. PubMed ID: 8077037
    [No Abstract]   [Full Text] [Related]  

  • 9. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes.
    Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT
    Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-inactivation pattern in an Ullrich-Turner syndrome patient with a small ring X and normal intelligence.
    Zenger-Hain JL; Wiktor A; Goldman J; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Sep; 47(4):490-3. PubMed ID: 8256812
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A boy with small supernumerary marker chromosome X identified by FISH.
    Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
    Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
    Lin CC; Meyne J; Sasi R; Bowen P; Unger T; Tainaka T; Hadro TA; Hoo JJ
    Am J Med Genet; 1990 Sep; 37(1):71-8. PubMed ID: 2240047
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
    Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular analysis of an idic(Y)(qter -->p11.32::p11.32-->qter) chromosome from a female patient with a complex karyotype.
    Fernandez R; Pasaro E
    Genet Mol Res; 2006 Jun; 5(2):399-406. PubMed ID: 16819718
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
    Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
    Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
    Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
    Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).
    Wiktor A; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jan; 45(1):22-4. PubMed ID: 8418653
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Detection of mosaicism in women with Turner's syndrome using fluorescence in situ hybridization].
    Zemanová Z; Musilová J; Kurková S; Mayerová K; Pacovská K; Michalová K
    Cas Lek Cesk; 1999 Jun; 138(13):396-400. PubMed ID: 10566209
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studies.
    Reddy KS; Smith DL; Ball CS
    Ann Genet; 1999; 42(2):105-8. PubMed ID: 10434125
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.