Dahl N - Search Results

1

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site.

Hirst MC, Bell MV, MacKinnon RN, Watson JE, Callen D, Sutherland G, Dahl N, Patterson MN, Schwartz C, Ledbetter D, et al. Hirst MC, et al. Among authors: dahl n. Am J Med Genet. 1991 Feb-Mar;38(2-3):354-6. doi: 10.1002/ajmg.1320380238. Am J Med Genet. 1991. PMID: 1673311

2

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Among authors: dahl n. Am J Hum Genet. 1991 Mar;48(3):460-7. Am J Hum Genet. 1991. PMID: 1671806 Free PMC article.

3

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

4

Linkage homogeneity near the fragile X locus in normal and fragile X families.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Among authors: dahl n. Genomics. 1991 Jul;10(3):576-82. doi: 10.1016/0888-7543(91)90438-k. Genomics. 1991. PMID: 1889808

5

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

6

Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.

van Oost BA, Smits A, Dreesen JC, Smeets D, Perdon L, van Bennekom CA, Dahl N, Bakker E, Oostra BA. van Oost BA, et al. Among authors: dahl n. Am J Med Genet. 1991 Feb-Mar;38(2-3):328-31. doi: 10.1002/ajmg.1320380232. Am J Med Genet. 1991. PMID: 2018075

7

Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type II.

Beck M, Steglich C, Zabel B, Dahl N, Schwinger E, Hopwood JJ, Gal A. Beck M, et al. Among authors: dahl n. Am J Med Genet. 1992 Sep 1;44(1):100-3. doi: 10.1002/ajmg.1320440123. Am J Med Genet. 1992. PMID: 1355630

8

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

9

X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).

Dahl N, Samson F, Thomas NS, Hu LJ, Gong W, Herman G, Laporte J, Kioschis P, Poustka A, Mandel JL. Dahl N, et al. J Med Genet. 1994 Dec;31(12):922-4. doi: 10.1136/jmg.31.12.922. J Med Genet. 1994. PMID: 7891372 Free PMC article.

10

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.

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

471 results

Search Page

Filters