Dahl N - Search Results

1

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. Among authors: dahl n. Am J Med Genet. 1991 Feb-Mar;38(2-3):322-7. doi: 10.1002/ajmg.1320380231. Am J Med Genet. 1991. PMID: 1673305

2

Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304.

Dahl N, Malmgren H, Pettersson U, Holmgren G, Seemanová E, Gustavson KH. Dahl N, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):319-21. doi: 10.1002/ajmg.1320380230. Am J Med Genet. 1991. PMID: 1673304

3

Molecular characterization of a DNA probe, U6.2, located close to the fragile X locus.

Pergolizzi R, Brown WT, Goonewardena P, Bhan R, Dobkin C, Dahl N, Pettersson U. Pergolizzi R, et al. Among authors: dahl n. Am J Med Genet. 1991 Feb-Mar;38(2-3):380-3. doi: 10.1002/ajmg.1320380245. Am J Med Genet. 1991. PMID: 1673315

4

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

5

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

6

DNA linkage analysis of X-linked retinoschisis.

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

7

Infantile autism--fragile X: molecular findings support genetic heterogeneity.

Malmgren H, Gustavson KH, Wahlström J, Arpi-Henriksson I, Bensch J, Pettersson U, Dahl N. Malmgren H, et al. Among authors: dahl n. Am J Med Genet. 1992 Dec 1;44(6):830-3. doi: 10.1002/ajmg.1320440624. Am J Med Genet. 1992. PMID: 1481857

8

Methylation and mutation patterns in the fragile X syndrome.

Malmgren H, Steén-Bondeson ML, Gustavson KH, Seémanova E, Holmgren G, Oberlé I, Mandel JL, Pettersson U, Dahl N. Malmgren H, et al. Among authors: dahl n. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):268-78. doi: 10.1002/ajmg.1320430142. Am J Med Genet. 1992. PMID: 1605200

9

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

10

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: dahl n. Am J Hum Genet. 1990 Jan;46(1):120-5. Am J Hum Genet. 1990. PMID: 1967204 Free PMC article.

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