Malmgren H - Search Results

1

The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.

Vincent A, Dahl N, Oberlé I, Hanauer A, Mandel JL, Malmgren H, Pettersson U. Vincent A, et al. Among authors: malmgren h. Genomics. 1989 Nov;5(4):797-801. doi: 10.1016/0888-7543(89)90121-3. Genomics. 1989. PMID: 2574147

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. 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: malmgren h. 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

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

5

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. Am J Med Genet. 1992 Dec 1;44(6):830-3. doi: 10.1002/ajmg.1320440624. Am J Med Genet. 1992. PMID: 1481857

6

[New genetic findings radically improve the diagnostic possibilities in fragile X syndrome].

Dahl N, Gustavson KH, Malmgren H, Pettersson U. Dahl N, et al. Among authors: malmgren h. Lakartidningen. 1992 Jun 3;89(23):2091-3. Lakartidningen. 1992. PMID: 1630231 Review. Swedish. No abstract available.

7

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Rousseau F, Heitz D, Tarleton J, MacPherson J, Malmgren H, Dahl N, Barnicoat A, Mathew C, Mornet E, Tejada I, et al. Rousseau F, et al. Among authors: malmgren h. Am J Hum Genet. 1994 Aug;55(2):225-37. Am J Hum Genet. 1994. PMID: 8037202 Free PMC article. Clinical Trial.

8

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. Eur J Hum Genet. 1994;2(2):103-9. doi: 10.1159/000472350. Eur J Hum Genet. 1994. PMID: 8044655

9

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

10

Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.

Bondeson ML, Dahl N, Malmgren H, Kleijer WJ, Tönnesen T, Carlberg BM, Pettersson U. Bondeson ML, et al. Among authors: malmgren h. Hum Mol Genet. 1995 Apr;4(4):615-21. doi: 10.1093/hmg/4.4.615. Hum Mol Genet. 1995. PMID: 7633410

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