Goonewardena P - Search Results

1

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: goonewardena p. Am J Hum Genet. 1989 Aug;45(2):304-9. Am J Hum Genet. 1989. PMID: 2569270 Free PMC article.

2

Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.

Goonewardena P, Brown WT, Gross AC, Ferrando C, Dobkin C, Romano V, Bosco P, Ceratto N, Pettersson U, Dahl N. Goonewardena P, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):322-7. doi: 10.1002/ajmg.1320380231. Am J Med Genet. 1991. PMID: 1673305

3

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: goonewardena p. Clin Genet. 1991 Dec;40(6):435-40. doi: 10.1111/j.1399-0004.1991.tb03115.x. Clin Genet. 1991. PMID: 1685699

4

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. Clin Genet. 1989 Jan;35(1):5-12. doi: 10.1111/j.1399-0004.1989.tb02899.x. Clin Genet. 1989. PMID: 2564327

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

6

Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes.

Goonewardena P, Gustavson KH, Holmgren G, Tolun A, Chotai J, Johnsen E, Pettersson U. Goonewardena P, et al. Clin Genet. 1986 Oct;30(4):249-54. doi: 10.1111/j.1399-0004.1986.tb00604.x. Clin Genet. 1986. PMID: 2878749

7

DNA linkage analysis of X-linked retinoschisis.

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

8

DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.

Goonewardena P, Dahl N, Gustavson KH, Holmgren G, Pettersson U. Goonewardena P, et al. Ups J Med Sci Suppl. 1987;44:155-64. Ups J Med Sci Suppl. 1987. PMID: 2895524

9

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. Genomics. 1988 Feb;2(2):115-8. doi: 10.1016/0888-7543(88)90092-4. Genomics. 1988. PMID: 2900806

10

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. Clin Genet. 1988 Nov;34(5):299-305. doi: 10.1111/j.1399-0004.1988.tb02882.x. Clin Genet. 1988. PMID: 3228998

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