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 *

127 related articles for article (PubMed ID: 468255)

  • 1. Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis.
    Laća Z; Ivanović M; Dramusić V; Morić-Petrović S
    Hum Genet; 1979 Jun; 49(2):237-41. PubMed ID: 468255
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X-X translocation in a patient with gonadal dysgenesis and the problems of phenotype-karyotype correlations.
    Mirzayants GG; Baranovskaya LI
    Hum Genet; 1978 Feb; 40(3):249-57. PubMed ID: 631846
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome.
    Barnes IC; Curtis DJ; Duncan SL
    J Med Genet; 1987 Jul; 24(7):428-31. PubMed ID: 3612719
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A teen-ager with 46,X,del(X)(q21).
    Srivastava PK; Fristoe F; McDavid RE; Townsend JF
    South Med J; 1979 Nov; 72(11):1461-3. PubMed ID: 505084
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosome.
    de la Chapelle A; Grönman P; Latt SA
    Cytogenet Cell Genet; 1978; 20(1-6):204-12. PubMed ID: 348409
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X inactivation pattern in an unbalanced X-autosome translocation with gonadal dysgenesis.
    Gaál M; László J
    Hum Hered; 1977; 27(6):396-402. PubMed ID: 908575
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern.
    Robertson J; Faed MJ; Lamont MA; Crowder AM
    J Med Genet; 1982 Dec; 19(6):463-5. PubMed ID: 7154045
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Primary amenorrhea with a new mosaic 46,XXqi/47,XXqi Xp-. Consideration on the X isochromosome formation and X chromosome inactivation.
    Halbrecht I; Shabtai F; Kuperstain C
    Acta Genet Med Gemellol (Roma); 1977; 26(1):63-9. PubMed ID: 71839
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structural aberration of the X chromosome in a patient with gonadal dysgenesis: an approach to karyotype-phenotype correlation.
    Varella-Garcia M; Tajara EH; Gagliardi AR
    J Med Genet; 1981 Jun; 18(3):228-31. PubMed ID: 7241547
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Sex chromosome aberrations in patients with menstruation disorders].
    Midro AT; Panasiuk B; Radwan J; Sipowicz I; Jaworowska B; Korsak E
    J Gynecol Obstet Biol Reprod (Paris); 1990; 19(7):811-6. PubMed ID: 2277162
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial short arm deletion of the X chromosome 46,X,del(X)(qter = to p21:).
    Käosaar M; Mikelsaar AV
    Hum Genet; 1980 Feb; 53(2):275-7. PubMed ID: 7358395
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. 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]  

  • 14. Fusion of the short arms of one X chromosome in a patient with gonadal dysgenesis.
    Ruthner U; Golob E
    Humangenetik; 1974; 24(2):159-60. PubMed ID: 4430496
    [No Abstract]   [Full Text] [Related]  

  • 15. Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations.
    Ferraro M; De Capoa A; Mostacci C; Pelliccia F; Zulli P; Baldini MA; Di Nisio Q
    J Med Genet; 1980 Dec; 17(6):457-63. PubMed ID: 7205428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cytogenetic studies in primary amenorrhea].
    Baron J; Warenik-Szymankiewicz A
    Zentralbl Gynakol; 1975; 97(11):649-55. PubMed ID: 1189755
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. X/X translocation in a girl with gonadal dysgenesis.
    Ishitobi K; Harada R; Ninomiya T; Santo Y; Harada Y
    Yonago Acta Med; 1976 Apr; 20(1):19-27. PubMed ID: 1025924
    [No Abstract]   [Full Text] [Related]  

  • 19. X short-arm deletion gonadal dysgenesis in two sibs.
    Davis JR; Heine MW; Graap RF; Lightner ES; Giles HR
    Birth Defects Orig Artic Ser; 1976; 12(5):137-8. PubMed ID: 953214
    [No Abstract]   [Full Text] [Related]  

  • 20. A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique.
    Crolla JA; Llerena JC
    Hum Genet; 1988 Dec; 81(1):81-4. PubMed ID: 3198130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.