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 *

103 related articles for article (PubMed ID: 1685701)

  • 1. Diagnostic reliability of the cytogenetic centromere heteromorphism in the human X chromosome.
    Friedrich U; Larsen TB; Nielsen J
    Clin Genet; 1991 Dec; 40(6):465-6. PubMed ID: 1685701
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular cytogenetic study of Turner's syndrome with the 45, X/46,X,r(?) karyotype].
    Shi Y; Shi H; Ma S
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1994 Jun; 16(3):218-21. PubMed ID: 7805169
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome.
    Maeda T; Ohno M; Takada M; Nishida M; Tsukioka K; Tomita H
    Clin Genet; 1979 Mar; 15(3):259-66. PubMed ID: 421365
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular studies of the parental origin and nature of human X isochromosomes.
    Harbison M; Hassold T; Kobryn C; Jacobs PA
    Cytogenet Cell Genet; 1988; 47(4):217-22. PubMed ID: 2901328
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Sex chromosome marker: clinical significance and DNA characterization.
    Johnson VP; McDonough PG; Cheung SW; Sun L
    Am J Med Genet; 1991 Apr; 39(1):97-101. PubMed ID: 1867271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Cytogenetic and molecular findings in patients with Turner's syndrome stigmata.
    Kuznetzova T; Baranov A; Schwed N; Ivaschenko T; Malet P; Giollant M; Savitsky GA; Baranov V
    J Med Genet; 1995 Dec; 32(12):962-7. PubMed ID: 8825925
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X chromosome instability associated with familial Turner syndrome.
    Tyrkus M; Hoffman WH; Kraemer-Flynn KM
    Clin Genet; 1989 Feb; 35(2):111-5. PubMed ID: 2721019
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A cytogenetic and molecular study of a series of 45,X fetuses and their parents.
    Cockwell A; MacKenzie M; Youings S; Jacobs P
    J Med Genet; 1991 Mar; 28(3):151-5. PubMed ID: 1675683
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stable dicentric X chromosomes with two functional centromeres.
    Sullivan BA; Willard HF
    Nat Genet; 1998 Nov; 20(3):227-8. PubMed ID: 9806536
    [No Abstract]   [Full Text] [Related]  

  • 12. Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation.
    Pinto MR; Leite RP; Areias A
    J Med Genet; 1989 Dec; 26(12):778-80. PubMed ID: 2614798
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular diagnosis of Turner's syndrome.
    Gicquel C; Cabrol S; Schneid H; Girard F; Le Bouc Y
    J Med Genet; 1992 Aug; 29(8):547-51. PubMed ID: 1355559
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.
    Koch J; Kølvraa S; Hobolt N; Petersen GB; Willard HF; Waye JS; Gregersen N; Bolund L
    Clin Genet; 1990 Mar; 37(3):216-20. PubMed ID: 2323091
    [TBL] [Abstract][Full Text] [Related]  

  • 15. G-11 staining in Turner's syndrome with mos 45,X/46,X,r(?).
    de Almeida JC; Llerena JC; Molina Gomes D; Rita Martins R; Jung M; Reis DF; Cunha AG
    Ann Genet; 1985; 28(1):37-41. PubMed ID: 2409888
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.
    Chelly J; Marlhens F; Le Marec B; Jeanpierre M; Lambert M; Hamard G; Dutrillaux B; Kaplan JC
    Hum Genet; 1986 Oct; 74(2):193-6. PubMed ID: 2876949
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes.
    Cooper C; Crolla JA; Laister C; Johnston DI; Cooke P
    J Med Genet; 1991 Jan; 28(1):6-9. PubMed ID: 1999837
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome.
    Binder G; Eggermann T; Enders H; Ranke MB; Dufke A
    J Pediatr; 2001 Feb; 138(2):285-7. PubMed ID: 11174634
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Study of isochromosomes of the long arms of the X chromosome].
    Borrego S; Fernández-Novoa C; San Martín V; Novales A; Hevia A; Galera H
    An Esp Pediatr; 1988 Aug; 29(2):117-21. PubMed ID: 3190016
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.