Holmgren G - Search Results

1

Strong founder effect for the fragile X syndrome in Sweden.

Malmgren H, Gustavson KH, Oudet C, Holmgren G, Pettersson U, Dahl N. Malmgren H, et al. Among authors: holmgren g. Eur J Hum Genet. 1994;2(2):103-9. doi: 10.1159/000472350. Eur J Hum Genet. 1994. PMID: 8044655

2

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: holmgren g. 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

3

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. Among authors: holmgren g. Am J Med Genet. 1991 Feb-Mar;38(2-3):319-21. doi: 10.1002/ajmg.1320380230. Am J Med Genet. 1991. PMID: 1673304

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

6

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. Among authors: holmgren g. Ups J Med Sci Suppl. 1987;44:155-64. Ups J Med Sci Suppl. 1987. PMID: 2895524

7

Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th century.

Holmgren G, Blomquist HK, Drugge U, Gustavson KH. Holmgren G, et al. Am J Med Genet. 1988 May-Jun;30(1-2):673-9. doi: 10.1002/ajmg.1320300168. Am J Med Genet. 1988. PMID: 3052071

8

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family.

Forsman K, Graff C, Nordström S, Johansson K, Westermark E, Lundgren E, Gustavson KH, Wadelius C, Holmgren G. Forsman K, et al. Among authors: holmgren g. Clin Genet. 1992 Sep;42(3):156-9. doi: 10.1111/j.1399-0004.1992.tb03229.x. Clin Genet. 1992. PMID: 1395087

9

Study of individuals possibly affected with the fragile X syndrome in a large Swedish family in the 18th to 20th centuries.

Drugge U, Holmgren G, Blomquist HK, Dahl N, Gustavson KH, Malmgren H. Drugge U, et al. Among authors: holmgren g. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):353-4. doi: 10.1002/ajmg.1320430154. Am J Med Genet. 1992. PMID: 1605211 No abstract available.

10

Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth century.

Drugge U, Blomquist HK, Gustavson KH, Holmgren G. Drugge U, et al. Among authors: holmgren g. Am J Med Genet. 1991 Feb-Mar;38(2-3):363-6. doi: 10.1002/ajmg.1320380240. Am J Med Genet. 1991. PMID: 2018076

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