Wadelius C - Search Results

1

Linkage analysis in properdin deficiency families: refined location in proximal Xp.

Wadelius C, Pigg M, Sundvall M, Sjöholm AG, Goonewardena P, Kuijper EJ, Tijssen CC, Jansz A, Späth PJ, Schaad UB, et al. Wadelius C, et al. Clin Genet. 1992 Jul;42(1):8-12. doi: 10.1111/j.1399-0004.1992.tb03126.x. Clin Genet. 1992. PMID: 1516231

2

Hemophilia B in a 46,XX female probably caused by non-random X inactivation.

Wadelius C, Lindstedt M, Pigg M, Egberg N, Pettersson U, Anvret M. Wadelius C, et al. Clin Genet. 1993 Jan;43(1):1-4. doi: 10.1111/j.1399-0004.1993.tb04415.x. Clin Genet. 1993. PMID: 8096443

3

Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome.

Dahl N, Hammarström-Heeroma K, Goonewardena P, Wadelius C, Gustavson KH, Holmgren G, van Ommen GJ, Pettersson U. Dahl N, et al. Among authors: wadelius c. Hum Genet. 1989 Jun;82(3):216-8. doi: 10.1007/BF00291157. Hum Genet. 1989. PMID: 2567272

4

The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic association.

Pigg M, Jagell S, Sillén A, Weissenbach J, Gustavson KH, Wadelius C. Pigg M, et al. Among authors: wadelius c. Nat Genet. 1994 Dec;8(4):361-4. doi: 10.1038/ng1294-361. Nat Genet. 1994. PMID: 7894487

5

Linkage mapping of a severe X-linked mental retardation syndrome.

Malmgren H, Sundvall M, Dahl N, Gustavson KH, Annerén G, Wadelius C, Steén-Bondeson ML, Pettersson U. Malmgren H, et al. Among authors: wadelius c. Am J Hum Genet. 1993 Jun;52(6):1046-52. Am J Hum Genet. 1993. PMID: 8503440 Free PMC article.

6

Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit gene.

Sillén A, Wadelius C, Sundvall M, Ahlsten G, Gustavson KH. Sillén A, et al. Among authors: wadelius c. Genet Couns. 1996;7(4):267-75. Genet Couns. 1996. PMID: 8985730

7

Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n).

Späth PJ, Sjöholm AG, Fredrikson GN, Misiano G, Scherz R, Schaad UB, Uhring-Lambert B, Hauptmann G, Westberg J, Uhlén M, Wadelius C, Truedsson L. Späth PJ, et al. Among authors: wadelius c. Clin Exp Immunol. 1999 Nov;118(2):278-84. doi: 10.1046/j.1365-2249.1999.01056.x. Clin Exp Immunol. 1999. PMID: 10540191 Free PMC article.

8

Evaluation of DNA-based diagnosis for haemophilia A.

Wadelius C, Blombäck M, Goonewardena P, Anvret M, Lindstedt M, Gustavson KH, Pettersson U. Wadelius C, et al. Scand J Clin Lab Invest. 1991 Nov;51(7):625-33. doi: 10.1080/00365519109104573. Scand J Clin Lab Invest. 1991. PMID: 1810022

9

Detailed genetic and physical mapping in the Sjögren-Larsson syndrome gene region in 17p11.2.

Sillén A, Alderborn A, Pigg M, Jagell S, Wadelius C. Sillén A, et al. Among authors: wadelius c. Hereditas. 1998;128(3):245-50. doi: 10.1111/j.1601-5223.1998.00245.x. Hereditas. 1998. PMID: 9760873 Free article.

10

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Pigg M, Annton-Lamprecht I, Braun-Quentin C, Gustavson KH, Wadelius C. Pigg M, et al. Among authors: wadelius c. Acta Derm Venereol. 1999 Jan;79(1):41-3. doi: 10.1080/000155599750011688. Acta Derm Venereol. 1999. PMID: 10086857 Free article.

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