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 *

102 related articles for article (PubMed ID: 601863)

  • 1. [Human isodicentric X-chromosomes].
    Verlinskaia DK; Mashkova MV
    Tsitologiia; 1977 Nov; 19(11):1276-8. PubMed ID: 601863
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Telomeric fusion of the short arms of both X chromosomes in a patient presenting an atypical Turner syndrome].
    Pescia G; Jotterand-Bellomo M; Nguyen TH; Scholberg-Hermann B
    J Genet Hum; 1980 Dec; 28(4):131-40. PubMed ID: 7205197
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Replication patterns of three isodicentric X chromosomes and an X isochromosome in human lymphocytes.
    Dewald G; Spurbeck JL; Gordon H
    Am J Med Genet; 1978; 1(4):445-60. PubMed ID: 665728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic findings in 125 patients with Turner's syndrome and abnormal karyotypes.
    Coco R; Bergada C
    J Genet Hum; 1977 Jun; 25(2):95-107. PubMed ID: 915489
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of 45,X/46,X,dic(X)(qter----p22::p22----qter) with Turner's phenotype in a Japanese girl.
    Takenaka M; Teramoto H; Ueda K; Fujiwara A; Ohama K; Nishi Y
    Hiroshima J Med Sci; 1988 Jun; 37(2):51-5. PubMed ID: 3170251
    [No Abstract]   [Full Text] [Related]  

  • 6. [Isochromosome X with long branches in two patients with Turner's syndrome].
    Nikezić M; Jokanović R; Ajdarić B; Garzicić B; Necić S
    Srp Arh Celok Lek; 1978 May; 106(5):553-61. PubMed ID: 751241
    [No Abstract]   [Full Text] [Related]  

  • 7. Center for Barr body condensation. A case of Turner's syndrome with 45,X/46,X,dic(X) (Xqter leads to p22::p22 leads to qter).
    Sillesen I; Rasmussen K; Osterballe O; Nielsen J
    Hum Genet; 1976 Aug; 33(3):337-40. PubMed ID: 964996
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter).
    Fujita H; Tanigawa Y; Yoshida Y; Okada Y
    Hum Genet; 1977 Nov; 39(2):147-55. PubMed ID: 598825
    [No Abstract]   [Full Text] [Related]  

  • 9. A rare case of Turner's syndrome with 45,X/46,X,Dic (X) (qter----p11.1::p11.4----qter).
    Lüleci G; Hoşgör O; Karaüzüm S; Uner M
    Hereditas; 1990; 113(3):217-20. PubMed ID: 2093701
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 46, X, del (X) (p21) in a 14-year-old female with Turner signs, one streak and one normal ovary.
    Crisalli M; Cuoco C; Gimelli G; Monteverde R
    Ann Genet; 1981; 24(2):114-6. PubMed ID: 6977291
    [No Abstract]   [Full Text] [Related]  

  • 11. [Dicentric Yp chromosome as one of the reasons for the absence of fluorescence in human Y chromosome].
    Verlinskaia DK; Prozorova MV
    Tsitologiia; 1983 Jun; 25(6):696-8. PubMed ID: 6684338
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Familial occurrence of isodicentric X chromosomes with different breakpoints.
    Midro AT; Kulikowski M; Sawicka A; Panasiuk B; Korsak E
    Clin Genet; 1988 Sep; 34(3):153-60. PubMed ID: 3180502
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Structure-function features of the long-arm iso-X-chromosome of 45, X/46X, i(Xq) patients].
    Beniush VA; Baranovskaia LI; Mirzaiants GG
    Genetika; 1975; 11(12):102-9. PubMed ID: 1225750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An abnormal dicentric X chromosome in a patient with short stature and gonadal dysgenesis.
    Smith A; Donnelly PE; Elliott G; den Dulk G
    Ann Genet; 1979; 22(3):143-7. PubMed ID: 316668
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Variant Turner features in a female with X-isochromosome [46,X, i(Xq)]: is it a distinct clinical entity?
    Verma RS; Vedbrat S; Khan F; Dosik H
    Ann Genet; 1981; 24(1):57-60. PubMed ID: 6971622
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Karyological variants in Turner's syndrome].
    Zanoio L; Povia P; Amantea P
    Minerva Ginecol; 1978 Oct; 30(10):817-20. PubMed ID: 724156
    [No Abstract]   [Full Text] [Related]  

  • 18. X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere.
    Maraschio P; Scappaticci S; Ferrari E; Fraccaro M
    Ann Genet; 1977 Sep; 20(3):179-83. PubMed ID: 304701
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial Turner's syndrome in four girls with Xq duplication and Xp deficiency.
    Nielsen LB; Boczkowski K; Mikkelsen M; Dahl G; Andersen E
    Hum Genet; 1982; 61(1):12-7. PubMed ID: 7129418
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic investigation of six patients with X isochromosomes, i(Xq), and of two subjects with isodicentric X chromosomes, idic (Xq).
    Gaál M; László J; Bösze P
    Hum Genet; 1981; 58(4):362-5. PubMed ID: 7327558
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.