Pettersson U - Search Results

1

Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis.

Wadelius C, Fagerholm P, Pettersson U, Annerén G. Wadelius C, et al. Among authors: pettersson u. Am J Hum Genet. 1989 Feb;44(2):241-7. Am J Hum Genet. 1989. PMID: 2912070 Free PMC article.

2

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: pettersson u. Am J Hum Genet. 1993 Jun;52(6):1046-52. Am J Hum Genet. 1993. PMID: 8503440 Free PMC article.

3

Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype.

Ahlbom BE, Goetz P, Korenberg JR, Pettersson U, Seemanova E, Wadelius C, Zech L, Annerén G. Ahlbom BE, et al. Among authors: pettersson u. Am J Med Genet. 1996 Jun 28;63(4):566-72. doi: 10.1002/(SICI)1096-8628(19960628)63:4<566::AID-AJMG10>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826436

4

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. Among authors: pettersson u. Scand J Clin Lab Invest. 1991 Nov;51(7):625-33. doi: 10.1080/00365519109104573. Scand J Clin Lab Invest. 1991. PMID: 1810022

5

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: pettersson u. Hum Genet. 1989 Jun;82(3):216-8. doi: 10.1007/BF00291157. Hum Genet. 1989. PMID: 2567272

6

Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).

Dahl N, Goonewardena P, Malmgren H, Gustavson KH, Holmgren G, Seemanova E, Annerén G, Flood A, Pettersson U. Dahl N, et al. Among authors: pettersson u. Am J Hum Genet. 1989 Aug;45(2):304-9. Am J Hum Genet. 1989. PMID: 2569270 Free PMC article.

7

Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodies.

Wadelius C, Blombäck M, Pettersson U. Wadelius C, et al. Among authors: pettersson u. Hum Genet. 1988 Dec;81(1):13-7. doi: 10.1007/BF00283721. Hum Genet. 1988. PMID: 2848757

8

DNA linkage analysis of X-linked retinoschisis.

Dahl N, Goonewardena P, Chotai J, Anvret M, Pettersson U. Dahl N, et al. Among authors: pettersson u. Hum Genet. 1988 Mar;78(3):228-32. doi: 10.1007/BF00291666. Hum Genet. 1988. PMID: 2894345

9

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. Among authors: pettersson u. Clin Genet. 1993 Jan;43(1):1-4. doi: 10.1111/j.1399-0004.1993.tb04415.x. Clin Genet. 1993. PMID: 8096443

10

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.

Arnell H, Hjälmås K, Jägervall M, Läckgren G, Stenberg A, Bengtsson B, Wassén C, Emahazion T, Annerén G, Pettersson U, Sundvall M, Dahl N. Arnell H, et al. Among authors: pettersson u. J Med Genet. 1997 May;34(5):360-5. doi: 10.1136/jmg.34.5.360. J Med Genet. 1997. PMID: 9152831 Free PMC article.

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