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 *

250 related articles for article (PubMed ID: 1733163)

  • 1. Noninactivation of a portion of Xq28 in a balanced X-autosome translocation.
    Du Sart D; Kalitsis P; Schmidt M
    Am J Med Genet; 1992 Jan; 42(2):156-60. PubMed ID: 1733163
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional disomies of the X chromosome influence the cell selection and hence the X inactivation pattern in females with balanced X-autosome translocations: a review of 122 cases.
    Schmidt M; Du Sart D
    Am J Med Genet; 1992 Jan; 42(2):161-9. PubMed ID: 1733164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.
    Sefiani A; Heuertz S; Turleau C; Thibaud D; de Grouchy J; Hors-Cayla MC
    Ann Genet; 1989; 32(3):149-51. PubMed ID: 2817774
    [TBL] [Abstract][Full Text] [Related]  

  • 4. H-Y antigen in human X-autosome translocations.
    Mayerova A; Zuffardi O; Maraschio P; Muller U; Sperling K; Ropers HH; Fraccaro M; Wolf U
    Acta Anthropogenet; 1983; 7(2):119-31. PubMed ID: 6611162
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.
    Wolff DJ; Schwartz S; Montgomery T; Zackowski JL
    Am J Med Genet; 1998 Jun; 77(5):401-4. PubMed ID: 9632170
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spreading of inactivation in an (X;14) translocation.
    Allderdice PW; Miller OJ; Miller DA; Klinger HP
    Am J Med Genet; 1978; 2(3):233-40. PubMed ID: 263441
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma.
    Stambolian D; Sellinger B; Derrington D; Sargent R; Emanuel BS
    Am J Med Genet; 1992 Apr; 42(6):771-6. PubMed ID: 1554012
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation.
    Sharp A; Robinson DO; Jacobs P
    Hum Genet; 2001 Sep; 109(3):295-302. PubMed ID: 11702210
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)].
    Gilgenkrantz S; Mauuary G; Dutrillaux B; Masocco G
    Humangenetik; 1975; 26(1):24-34. PubMed ID: 50264
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.
    Zori RT; Gray BA; Bent-Williams A; Driscoll DJ; Williams CA; Zackowski JL
    Am J Med Genet; 1993 Jun; 46(4):379-83. PubMed ID: 8357008
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spatial distribution of histone isoforms on the bovine active and inactive X chromosomes.
    Coppola G; Pinton A; Joudrey EM; Basrur PK; King WA
    Sex Dev; 2008; 2(1):12-23. PubMed ID: 18418031
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aarskog syndrome: full male and female expression associated with an X-autosome translocation.
    Bawle E; Tyrkus M; Lipman S; Bozimowski D
    Am J Med Genet; 1984 Mar; 17(3):595-602. PubMed ID: 6711610
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lack of X inactivation: loss of one X inactivation center in a case with mos45,X,-21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2).
    Ishikiriyama S; Iai M; Tanabe Y
    Am J Med Genet; 1993 Aug; 47(1):41-4. PubMed ID: 8368250
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.
    Bienvenu T; Der-Sarkissian H; Billuart P; Tissot M; Des Portes V; Brüls T; Chabrolle JP; Chauveau P; Cherry M; Kahn A; Cohen D; Beldjord C; Chelly J; Cherif D
    Eur J Hum Genet; 1997; 5(2):105-9. PubMed ID: 9195162
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Clinical case of tandem translocation between chromosomes 13 and 15].
    Badalian LO; Arkhipov BA; Malygina NA; Patrukhin AS; Lysov VL
    Tsitol Genet; 1985; 19(4):304-8. PubMed ID: 4049521
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivation.
    Preis W; Barbi G; Liptay S; Kennerknecht I; Schwemmle S; Pohlandt F
    Am J Med Genet; 1996 Jan; 61(2):117-21. PubMed ID: 8669435
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple congenital anomalies in a man with (X;6) translocation.
    Sivak LE; Esbenshade J; Brothman AR; Issa B; Lemons RS; Carey JC
    Am J Med Genet; 1994 May; 51(1):9-12. PubMed ID: 8030680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Investigation of the "variable spreading" of X inactivation into a translocated autosome.
    Schanz S; Steinbach P
    Hum Genet; 1989 Jun; 82(3):244-8. PubMed ID: 2731936
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Secondary amenorrhea associated with balanced X-autosome translocation.
    Sauer F; Greenstein RM; Reardon P; Riddick DH
    Obstet Gynecol; 1977 Jan; 49(1):101-4. PubMed ID: 831158
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A teenager with a t(X;17)(q22;q25) and ovarian failure.
    Martínez-Valenzuela M; Rivera H; Mundo-Ayala JN; González-Mercado MG; Davalos-Rodríguez IP
    Genet Couns; 2010; 21(3):269-75. PubMed ID: 20964116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.