Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

244 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
Cossée M, Dürr A, Schmitt M, Dahl N, Trouillas P, Allinson P, Kostrzewa M, Nivelon-Chevallier A, Gustavson KH, Kohlschütter A, Müller U, Mandel JL, Brice A, Koenig M, Cavalcanti F, Tammaro A, De Michele G, Filla A, Cocozza S, Labuda M, Montermini L, Poirier J, Pandolfo M. Cossée M, et al. Among authors: gustavson kh. Ann Neurol. 1999 Feb;45(2):200-6. doi: 10.1002/1531-8249(199902)45:2<200::aid-ana10>3.0.co;2-u. Ann Neurol. 1999. PMID: 9989622
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: gustavson kh. 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
Re-evaluation of the dysequilibrium syndrome.
Melberg A, Orlén H, Raininko R, Entesarian M, Dahlqvist J, Gustavson KH, Dahl N. Melberg A, et al. Among authors: gustavson kh. Acta Neurol Scand. 2011 Jan;123(1):28-33. doi: 10.1111/j.1600-0404.2010.01335.x. Acta Neurol Scand. 2011. PMID: 20199520
A case of complete trisomy 2p/triploidy mosaicism.
Dahl N, Eliasson IL, Gustavson KH. Dahl N, et al. Among authors: gustavson kh. Acta Paediatr Scand. 1988 Nov;77(6):925-9. doi: 10.1111/j.1651-2227.1988.tb10785.x. Acta Paediatr Scand. 1988. PMID: 3207029
[Molecular genetic diagnostics--experiences from Uppsala].
Annerén G, Dahl N, Gustavson KH, Pettersson U, Wadelius C. Annerén G, et al. Among authors: gustavson kh. Lakartidningen. 1988 Jun 15;85(24):2186, 2188, 2191-2. Lakartidningen. 1988. PMID: 3290601 Swedish. No abstract available.
Benign ovarian teratomas. An analysis of their cellular origin.
Dahl N, Gustavson KH, Rune C, Gustavsson I, Pettersson U. Dahl N, et al. Among authors: gustavson kh. Cancer Genet Cytogenet. 1990 May;46(1):115-23. doi: 10.1016/0165-4608(90)90017-5. Cancer Genet Cytogenet. 1990. PMID: 1970513
Multiple epiphyseal dysplasia.
Dahlqvist J, Orlén H, Matsson H, Dahl N, Lönnerholm T, Gustavson KH. Dahlqvist J, et al. Among authors: gustavson kh. Acta Orthop. 2009 Dec;80(6):711-5. doi: 10.3109/17453670903473032. Acta Orthop. 2009. PMID: 19995321 Free PMC article.
244 results