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 *

170 related articles for article (PubMed ID: 2895261)

  • 1. Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiency.
    Goodship J; Malcolm S; Lau YL; Pembrey ME; Levinsky RJ
    Lancet; 1988 Apr; 1(8588):729-32. PubMed ID: 2895261
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Carrier detection in the Wiskott Aldrich syndrome.
    Fearon ER; Kohn DB; Winkelstein JA; Vogelstein B; Blaese RM
    Blood; 1988 Nov; 72(5):1735-9. PubMed ID: 3263154
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus.
    Hendriks RW; Kraakman ME; Schuurman RK
    Clin Genet; 1992 Sep; 42(3):114-21. PubMed ID: 1395081
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect.
    Greer WL; Kwong PC; Peacocke M; Ip P; Rubin LA; Siminovitch KA
    Genomics; 1989 Jan; 4(1):60-7. PubMed ID: 2563352
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation.
    Puck JM; Nussbaum RL; Conley ME
    J Clin Invest; 1987 May; 79(5):1395-400. PubMed ID: 2883199
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.
    Goodship J; Levinsky R; Malcolm S
    Hum Genet; 1989 Dec; 84(1):11-4. PubMed ID: 2606471
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.
    Tsuge I; Matsuoka H; Abe T; Kamachi Y; Torii S
    Eur J Pediatr; 1993 Nov; 152(11):900-4. PubMed ID: 8276019
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders.
    Puck JM
    Pediatr Res; 1993 Jan; 33(1 Suppl):S29-33; discussion S33-4. PubMed ID: 8433872
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.
    Conley ME; Lavoie A; Briggs C; Brown P; Guerra C; Puck JM
    Proc Natl Acad Sci U S A; 1988 May; 85(9):3090-4. PubMed ID: 2896355
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.
    Lester T; de Alwis M; Clark PA; Jones AM; Katz F; Levinsky RJ; Kinnon C
    J Med Genet; 1994 Sep; 31(9):717-20. PubMed ID: 7815443
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.
    Puck JM; Nussbaum RL; Smead DL; Conley ME
    Am J Hum Genet; 1989 May; 44(5):724-30. PubMed ID: 2565084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytes.
    Goodship J; Malcolm S; Levinsky RJ
    Clin Exp Immunol; 1991 Jan; 83(1):4-9. PubMed ID: 1988230
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene.
    van Kamp H; Fibbe WE; Jansen RP; van der Keur M; de Graaff E; Willemze R; Landegent JE
    Blood; 1992 Oct; 80(7):1774-80. PubMed ID: 1356510
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Carrier detection in typical and atypical X-linked agammaglobulinemia.
    Conley ME; Puck JM
    J Pediatr; 1988 May; 112(5):688-94. PubMed ID: 2896233
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Carrier detection in agammaglobulinemia by X chromosome inactivation analysis.
    Miyashita T; Iwata T; Mizutani S; Kamoshita S; Kobayashi N
    Acta Paediatr Jpn; 1992 Jun; 34(3):267-72. PubMed ID: 1354911
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic study of a new X-linked recessive immunodeficiency syndrome.
    de Saint-Basile G; Le Deist F; Caniglia M; Lebranchu Y; Griscelli C; Fischer A
    J Clin Invest; 1992 Mar; 89(3):861-6. PubMed ID: 1347296
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: demonstration of heterogeneity in lineage involvement.
    Tsukamoto N; Morita K; Maehara T; Okamoto K; Sakai H; Karasawa M; Naruse T; Omine M
    Br J Haematol; 1994 Feb; 86(2):253-8. PubMed ID: 7911034
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages.
    Notarangelo LD; Parolini O; Albertini A; Duse M; Mazzolari E; Plebani A; Camerino G; Ugazio AG
    Hum Genet; 1991 Dec; 88(2):130-4. PubMed ID: 1757090
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X chromosome linked immunodeficiency.
    Schwaber J; Rosen FS
    Immunodefic Rev; 1990; 2(3):233-51. PubMed ID: 1981831
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probe.
    Goodship J; Carter J; Espanol T; Boyd Y; Malcolm S; Levinsky RJ
    Blood; 1991 Jun; 77(12):2677-81. PubMed ID: 2043768
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.