Dahl N - Search Results

1

Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden.

Melin M, Entesarian M, Carlsson G, Garwicz D, Klein C, Fadeel B, Nordenskjöld M, Palmblad J, Henter JI, Dahl N. Melin M, et al. Among authors: dahl n. Biochem Biophys Res Commun. 2007 Feb 16;353(3):571-5. doi: 10.1016/j.bbrc.2006.12.086. Epub 2006 Dec 20. Biochem Biophys Res Commun. 2007. PMID: 17188649 Free PMC article.

2

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.

Arnell H, Hjälmås K, Jägervall M, Läckgren G, Stenberg A, Bengtsson B, Wassén C, Emahazion T, Annerén G, Pettersson U, Sundvall M, Dahl N. Arnell H, et al. Among authors: dahl n. J Med Genet. 1997 May;34(5):360-5. doi: 10.1136/jmg.34.5.360. J Med Genet. 1997. PMID: 9152831 Free PMC article.

3

Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb.

Gustavsson P, Willing TN, van Haeringen A, Tchernia G, Dianzani I, Donnér M, Elinder G, Henter JI, Nilsson PG, Gordon L, Skeppner G, van't Veer-Korthof L, Kreuger A, Dahl N. Gustavsson P, et al. Among authors: dahl n. Nat Genet. 1997 Aug;16(4):368-71. doi: 10.1038/ng0897-368. Nat Genet. 1997. PMID: 9241274

4

Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.

Balciuniene J, Dahl N, Borg E, Samuelsson E, Koisti MJ, Pettersson U, Jazin EE. Balciuniene J, et al. Among authors: dahl n. Am J Hum Genet. 1998 Sep;63(3):786-93. doi: 10.1086/302012. Am J Hum Genet. 1998. PMID: 9718342 Free PMC article.

5

Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity.

Gustavsson P, Garelli E, Draptchinskaia N, Ball S, Willig TN, Tentler D, Dianzani I, Punnett HH, Shafer FE, Cario H, Ramenghi U, Glomstein A, Pfeiffer RA, Goringe A, Olivieri NF, Smibert E, Tchernia G, Elinder G, Dahl N. Gustavsson P, et al. Among authors: dahl n. Am J Hum Genet. 1998 Nov;63(5):1388-95. doi: 10.1086/302100. Am J Hum Genet. 1998. PMID: 9792865 Free PMC article.

6

Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.

Arnell H, Mäntyjärvi M, Tuppurainen K, Andréasson S, Dahl N. Arnell H, et al. Among authors: dahl n. Acta Ophthalmol Scand. 1998 Dec;76(6):649-52. doi: 10.1034/j.1600-0420.1998.760602.x. Acta Ophthalmol Scand. 1998. PMID: 9881544 Free article.

7

Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene.

Gustavsson P, Klar J, Matsson H, Forestier E, Henter JI, Rao S, Seip M, Skeppner G, Dahl N. Gustavsson P, et al. Among authors: dahl n. Br J Haematol. 2002 Oct;119(1):261-4. doi: 10.1046/j.1365-2141.2002.03776.x. Br J Haematol. 2002. PMID: 12358933 Free article.

8

Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands.

Entesarian M, Matsson H, Klar J, Bergendal B, Olson L, Arakaki R, Hayashi Y, Ohuchi H, Falahat B, Bolstad AI, Jonsson R, Wahren-Herlenius M, Dahl N. Entesarian M, et al. Among authors: dahl n. Nat Genet. 2005 Feb;37(2):125-7. doi: 10.1038/ng1507. Epub 2005 Jan 16. Nat Genet. 2005. PMID: 15654336

9

A Meniere's disease gene linked to chromosome 12p12.3.

Klar J, Frykholm C, Friberg U, Dahl N. Klar J, et al. Among authors: dahl n. Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 5;141B(5):463-7. doi: 10.1002/ajmg.b.30347. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16741942

10

Adult-onset autosomal dominant leukodystrophy with autonomic symptoms restricted to 1.5 Mbp on chromosome 5q23.

Marklund L, Melin M, Melberg A, Giedraitis V, Dahl N. Marklund L, et al. Among authors: dahl n. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):608-14. doi: 10.1002/ajmg.b.30342. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823806

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