188 related articles for article (PubMed ID: 2883112)
1. X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.
Mensink EJ; Thompson A; Sandkuyl LA; Kraakman ME; Schot JD; Espanol T; Schuurman RK
Hum Genet; 1987 May; 76(1):96-9. PubMed ID: 2883112
[TBL] [Abstract][Full Text] [Related]
2. Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact.
Hendriks RW; Kraakman ME; Craig IW; Espanol T; Schuurman RK
Eur J Immunol; 1990 Dec; 20(12):2603-8. PubMed ID: 1980111
[TBL] [Abstract][Full Text] [Related]
3. Mapping of the X linked form of hyper IgM syndrome (HIGM1).
Padayachee M; Levinsky RJ; Kinnon C; Finn A; McKeown C; Feighery C; Notarangelo LD; Hendriks RW; Read AP; Malcolm S
J Med Genet; 1993 Mar; 30(3):202-5. PubMed ID: 8097258
[TBL] [Abstract][Full Text] [Related]
4. Mapping the X-linked lymphoproliferative syndrome.
Skare JC; Milunsky A; Byron KS; Sullivan JL
Proc Natl Acad Sci U S A; 1987 Apr; 84(7):2015-8. PubMed ID: 2882515
[TBL] [Abstract][Full Text] [Related]
5. Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.
de Saint Basile G; Arveiler B; Oberlé I; Malcolm S; Levinsky RJ; Lau YL; Hofker M; Debre M; Fischer A; Griscelli C
Proc Natl Acad Sci U S A; 1987 Nov; 84(21):7576-9. PubMed ID: 3478714
[TBL] [Abstract][Full Text] [Related]
6. Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37.
Skare JC; Grierson HL; Sullivan JL; Nussbaum RL; Purtilo DT; Sylla BS; Lenoir GM; Reilly DS; White BN; Milunsky A
Hum Genet; 1989 Jul; 82(4):354-8. PubMed ID: 2567696
[TBL] [Abstract][Full Text] [Related]
7. Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.
Sylla BS; Wang Q; Hayoz D; Lathrop GM; Lenoir GM
Clin Genet; 1989 Dec; 36(6):459-62. PubMed ID: 2574086
[TBL] [Abstract][Full Text] [Related]
8. Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci.
Chen JD; Halliday F; Keith G; Sheffield L; Dickinson P; Gray R; Constable I; Denton M
Am J Hum Genet; 1989 Sep; 45(3):401-11. PubMed ID: 2570529
[TBL] [Abstract][Full Text] [Related]
9. Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.
Skare JC; Sullivan JL; Milunsky A
Hum Genet; 1989 Jul; 82(4):349-53. PubMed ID: 2567695
[TBL] [Abstract][Full Text] [Related]
10. Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity.
Mensink EJ; Thompson A; Schot JD; van de Greef WM; Sandkuyl LA; Schuurman RK
Hum Genet; 1986 Aug; 73(4):327-32. PubMed ID: 3502688
[TBL] [Abstract][Full Text] [Related]
11. Genetic heterogeneity in X-linked agammaglobulinemia complicates carrier detection and prenatal diagnosis.
Mensink EJ; Thompson A; Schot JD; Kraakman ME; Sandkuyl LA; Schuurman RK
Clin Genet; 1987 Feb; 31(2):91-6. PubMed ID: 2881637
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of X-linked immunodeficiency with hyper-IgM and X-linked lymphoproliferative syndrome.
Notarangelo LD; Mantuano E; Bione S; Gimbo E; Giliani S; Caraffini A; Purtilo D; Farr C; Ugazio AG; Toniolo D
Immunodeficiency; 1993; 4(1-4):225-9. PubMed ID: 8167706
[No Abstract] [Full Text] [Related]
13. X-linked lymphoproliferative disease: linkage studies using DNA probes.
Harris A; Lenoir GM; Lankester SA
Clin Genet; 1988 Mar; 33(3):162-8. PubMed ID: 2896078
[TBL] [Abstract][Full Text] [Related]
14. Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia M.
Kraakman ME; de Weers M; Español T; Schuurman RK; Hendriks RW
Clin Genet; 1995 Jul; 48(1):46-8. PubMed ID: 7586644
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. X-linked immunodeficiency with hyper-IgM (XHIM).
Notarangelo LD; Hayward AR
Clin Exp Immunol; 2000 Jun; 120(3):399-405. PubMed ID: 10844515
[No Abstract] [Full Text] [Related]
17. X chromosome linked immunodeficiency.
Schwaber J; Rosen FS
Immunodefic Rev; 1990; 2(3):233-51. PubMed ID: 1981831
[TBL] [Abstract][Full Text] [Related]
18. Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
Nussbaum RL; Lewis RA; Lesko JG; Ferrell R
Am J Hum Genet; 1985 May; 37(3):473-81. PubMed ID: 2988333
[TBL] [Abstract][Full Text] [Related]
19. Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosome.
Goonewardena P; Sjöholm AG; Nilsson LA; Pettersson U
Genomics; 1988 Feb; 2(2):115-8. PubMed ID: 2900806
[TBL] [Abstract][Full Text] [Related]
20. Eczematous skin lesions in X-linked immunodeficiency with hyper-IgM.
Vieluf D; Korting HC; Belohradsky BH
Curr Probl Dermatol; 1989; 18():60-5. PubMed ID: 2743804
[No Abstract] [Full Text] [Related]
[Next] [New Search]
