Pettersson U - Search Results

1

A linkage study of the locus for X-linked Charcot-Marie-Tooth disease.

Goonewardena P, Welihinda J, Anvret M, Gyftodimou J, Haegermark A, Iselius L, Lindsten J, Pettersson U. Goonewardena P, et al. Among authors: pettersson u. Clin Genet. 1988 Jun;33(6):435-40. doi: 10.1111/j.1399-0004.1988.tb03477.x. Clin Genet. 1988. PMID: 2901924

2

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

3

Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosome.

Goonewardena P, Sjöholm AG, Nilsson LA, Pettersson U. Goonewardena P, et al. Among authors: pettersson u. Genomics. 1988 Feb;2(2):115-8. doi: 10.1016/0888-7543(88)90092-4. Genomics. 1988. PMID: 2900806

4

A new type of muscular dystrophy in two brothers: analysis by use of DNA probes suggests autosomal recessive inheritance.

Goonewardena P, Gustavson KH, Gamstorp I, Lundström NR, Pettersson U. Goonewardena P, et al. Among authors: pettersson u. Clin Genet. 1988 Nov;34(5):299-305. doi: 10.1111/j.1399-0004.1988.tb02882.x. Clin Genet. 1988. PMID: 3228998

5

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

6

Genetic mapping of loci for X-linked retinitis pigmentosa.

Dahl N, Sundvall M, Pettersson U, Andréasson S, Anvret M, Kugelberg U, Hagbyhn-Gericke A, Goonewardena P. Dahl N, et al. Among authors: pettersson u. Clin Genet. 1991 Dec;40(6):435-40. doi: 10.1111/j.1399-0004.1991.tb03115.x. Clin Genet. 1991. PMID: 1685699

7

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

Lagerström M, Dahl N, Iselius L, Bäckman B, Pettersson U. Lagerström M, et al. Among authors: pettersson u. Am J Hum Genet. 1990 Jan;46(1):120-5. Am J Hum Genet. 1990. PMID: 1967204 Free PMC article.

8

Molecular Xp deletion in a male: suggestion of a locus for hypogonadotropic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci.

Goonewardena P, Dahl N, Ritzén M, van Ommen GJ, Pettersson U. Goonewardena P, et al. Among authors: pettersson u. Clin Genet. 1989 Jan;35(1):5-12. doi: 10.1111/j.1399-0004.1989.tb02899.x. Clin Genet. 1989. PMID: 2564327

9

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

10

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.

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