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Items: 1 to 20 of 312

1.

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
2.

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
3.
4.

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.

5.

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
6.

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
7.

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
8.

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.

9.

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Bleeker-Wagemakers LM, Friedrich U, Gal A, Wienker TF, Warburg M, Ropers HH.

Hum Genet. 1985;71(3):211-4.

PMID:
2998969
10.

A primary genetic map of the pericentromeric region of the human X chromosome.

Mahtani MM, Willard HF.

Genomics. 1988 May;2(4):294-301.

PMID:
2906040
11.

[Molecular genetic diagnosis of Wiskott-Aldrich syndrome].

Orth U, Rosenkranz W, Schwinger E, Holzgreve W, Gal A.

Monatsschr Kinderheilkd. 1993 Sep;141(9):728-31. German.

PMID:
8413349
12.

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
13.

The Wiskott-Aldrich syndrome.

Peacocke M, Siminovitch KA.

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

PMID:
8105860
14.
15.

[Genetic carrier detection for the Wiskott-Aldrich syndrome using restriction fragment length polymorphism analysis].

de Weers M, Kolvenbag GJ, Versteegde IF, Hendriks RW, Sandkuyl LA, Schuurman RK.

Ned Tijdschr Geneeskd. 1990 May 5;134(18):913-6. Dutch.

PMID:
1971711
16.

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.

Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM.

Hum Genet. 1989 Mar;81(4):315-8.

PMID:
2564836
17.

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.

18.
19.

Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis.

Lagerström M, Dahl N, Iselius L, Bäckman B, Pettersson U.

Am J Hum Genet. 1990 Jan;46(1):120-5.

20.

Localization of the X-linked retinitis pigmentosa locus between DXS7 and DXS84 in a family showing tapetal reflex in heterozygotes.

Chen JD, Halliday F, Serravalle S, Denton M.

Ophthalmic Paediatr Genet. 1988 Nov;9(3):143-7.

PMID:
2906743
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