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Items: 1 to 20 of 132

1.

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3.

Kwan SP, Lehner T, Hagemann T, Lu B, Blaese M, Ochs H, Wedgwood R, Ott J, Craig IW, Rosen FS.

Genomics. 1991 May;10(1):29-33.

PMID:
1675197
2.

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.

Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS.

Genomics. 1988 Jul;3(1):39-43.

PMID:
2906042
3.

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome.

Greer WL, Somani AK, Kwong PC, Peacocke M, Rubin LA, Siminovitch KA.

Genomics. 1990 Mar;6(3):568-71.

PMID:
2328995
4.

Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

Arveiler B, de Saint-Basile G, Fischer A, Griscelli C, Mandel JL.

Am J Hum Genet. 1990 May;46(5):906-11.

5.

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.

Musarella MA, Weleber RG, Murphey WH, Young RS, Anson-Cartwright L, Mets M, Kraft SP, Polemeno R, Litt M, Worton RG.

Genomics. 1989 Nov;5(4):727-37.

PMID:
2574143
6.

The Wiskott-Aldrich syndrome.

Peacocke M, Siminovitch KA.

Semin Dermatol. 1993 Sep;12(3):247-54.

PMID:
8105860
7.
8.

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.

Peacocke M, Siminovitch KA.

Proc Natl Acad Sci U S A. 1987 May;84(10):3430-3.

9.

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

Wright AF, Bhattacharya SS, Clayton JF, Dempster M, Tippett P, McKeown CM, Jay M, Jay B, Bird AC.

Am J Hum Genet. 1987 Oct;41(4):635-44.

10.

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.

J Clin Invest. 1993 Jun;91(6):2351-7.

11.

Genetic and physical mapping around the properdin P gene.

Coleman MP, Murray JC, Willard HF, Nolan KF, Reid KB, Blake DJ, Lindsay S, Bhattacharya SS, Wright A, Davies KE.

Genomics. 1991 Dec;11(4):991-6.

PMID:
1783405
12.

Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 region.

Cremin SM, Greer WL, Bodok-Nutzati R, Schwartz M, Peacocke M, Siminovitch KA.

Hum Genet. 1993 Oct 1;92(3):250-3.

PMID:
8104859
13.

Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome.

de Saint Basile G, Arveiler B, Fraser NJ, Boyd Y, Graig IW, Griscelli G, Fischer A.

Lancet. 1989 Dec 2;2(8675):1319-21.

PMID:
2574264
14.

Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Wright AF, Bhattacharya SS, Aldred MA, Jay M, Carothers AD, Thomas NS, Bird AC, Jay B, Evans HJ.

J Med Genet. 1991 Jul;28(7):453-7.

15.

X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3.

Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF.

Am J Hum Genet. 2000 Feb;66(2):461-8.

16.

Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus.

Hendriks RW, De Weers M, Mensink RG, Kraakman ME, Mollee-Versteegde IF, Veerman AJ, Sandkuyl LA, Schuurman RK.

Clin Exp Immunol. 1991 May;84(2):219-22.

17.

Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome.

Donnér M, Schwartz M, Carlsson KU, Holmberg L.

Blood. 1988 Dec;72(6):1849-53.

18.
19.

Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction.

Greer WL, Mahtani MM, Kwong PC, Rubin LA, Peacocke M, Willard HF, Siminovitch KA.

Hum Genet. 1989 Oct;83(3):227-30.

PMID:
2571560
20.

The UDP-galactose translocator gene is mapped to band Xp11.23-p11.22 containing the Wiskott-Aldrich syndrome locus.

Hara T, Yamauchi M, Takahashi E, Hoshino M, Aoki K, Ayusawa D, Kawakita M.

Somat Cell Mol Genet. 1993 Nov;19(6):571-5.

PMID:
8128316

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