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Items: 1 to 20 of 331

1.

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.

PMID:
3502688
2.

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.

PMID:
2881637
3.

X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked.

Mensink EJ, Schot JD, Tippett P, Ott J, Schuurman RK.

Hum Genet. 1984;68(4):303-9.

PMID:
6595200
4.

Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci.

Ott J, Mensink EJ, Thompson A, Schot JD, Schuurman RK.

Hum Genet. 1986 Nov;74(3):280-3.

PMID:
2877937
5.

Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.

Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F.

Genomics. 1990 Feb;6(2):238-42.

PMID:
2307467
6.

Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.

Guioli S, Arveiler B, Bardoni B, Notarangelo LD, Panina P, Duse M, Ugazio A, Oberlé I, de Saint Basile G, Mandel JL, et al.

Hum Genet. 1989 Dec;84(1):19-21.

PMID:
2575070
7.

Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).

Malcolm S, de Saint Basile G, Arveiler B, Lau YL, Szabo P, Fischer A, Griscelli C, Debre M, Mandel JL, Callard RE, et al.

Hum Genet. 1987 Oct;77(2):172-4.

PMID:
2888720
8.

Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia.

Hendriks RW, Mensink EJ, Kraakman ME, Thompson A, Schuurman RK.

Hum Genet. 1989 Oct;83(3):267-70.

PMID:
2571563
9.

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

Kwan SP, Kunkel L, Bruns G, Wedgwood RJ, Latt S, Rosen FS.

J Clin Invest. 1986 Feb;77(2):649-52.

10.

Genetic linkage heterogeneity in the fragile X syndrome.

Brown WT, Gross AC, Chan CB, Jenkins EC.

Hum Genet. 1985;71(1):11-8.

PMID:
2993154
11.

Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22.

Lovering R, Middleton-Price HR, O'Reilly MA, Genet SA, Parkar M, Sweatman AK, Bradley LD, Alterman LA, Malcolm S, Morgan G, et al.

Hum Mol Genet. 1993 Feb;2(2):139-41.

PMID:
8499902
12.

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.

13.

Carrier detection in typical and atypical X-linked agammaglobulinemia.

Conley ME, Puck JM.

J Pediatr. 1988 May;112(5):688-94.

PMID:
2896233
14.

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.

PMID:
2883112
15.

Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.

Parolini O, Hejtmancik JF, Allen RC, Belmont JW, Lassiter GL, Henry MJ, Barker DF, Conley ME.

Genomics. 1993 Feb;15(2):342-9.

PMID:
8449500
16.

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, et al.

Proc Natl Acad Sci U S A. 1987 Nov;84(21):7576-9.

17.
18.

Genetic heterogeneity in X-linked amelogenesis imperfecta.

Aldred MJ, Crawford PJ, Roberts E, Gillespie CM, Thomas NS, Fenton I, Sandkuijl LA, Harper PS.

Genomics. 1992 Nov;14(3):567-73.

PMID:
1358807
19.

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.

20.

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Argonza R, Tsui LC, Worton R.

Am J Hum Genet. 1988 Oct;43(4):484-94.

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