Pettersson U - Search Results

1

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: pettersson u. 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

2

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: pettersson u. Ups J Med Sci Suppl. 1987;44:155-64. Ups J Med Sci Suppl. 1987. PMID: 2895524

3

Use of linked DNA probes for carrier detection and diagnosis of X-linked juvenile retinoschisis.

Dahl N, Pettersson U. Dahl N, et al. Among authors: pettersson u. Arch Ophthalmol. 1988 Oct;106(10):1414-6. doi: 10.1001/archopht.1988.01060140578026. Arch Ophthalmol. 1988. PMID: 3178553

4

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

5

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

6

Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene.

Steén-Bondeson ML, Dahl N, Tönnesen T, Kleijer WJ, Seidlitz G, Gustavson KH, Wilson PJ, Morris CP, Hopwood JJ, Pettersson U. Steén-Bondeson ML, et al. Among authors: pettersson u. Hum Mol Genet. 1992 Jun;1(3):195-8. doi: 10.1093/hmg/1.3.195. Hum Mol Genet. 1992. PMID: 1303177

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

8

[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: pettersson u. Lakartidningen. 1992 Jun 3;89(23):2091-3. Lakartidningen. 1992. PMID: 1630231 Review. Swedish. No abstract available.

9

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

10

Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase gene.

Dahl N, Lagerström M, Erikson A, Pettersson U. Dahl N, et al. Among authors: pettersson u. Am J Hum Genet. 1990 Aug;47(2):275-8. Am J Hum Genet. 1990. PMID: 2378352 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

417 results

Search Page

Filters