Horn N - Search Results

1

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.

Chelly J, Tümer Z, Tønnesen T, Petterson A, Ishikawa-Brush Y, Tommerup N, Horn N, Monaco AP. Chelly J, et al. Among authors: horn n. Nat Genet. 1993 Jan;3(1):14-9. doi: 10.1038/ng0193-14. Nat Genet. 1993. PMID: 8490646

2

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.

Tümer Z, Chelly J, Tommerup N, Ishikawa-Brush Y, Tønnesen T, Monaco AP, Horn N. Tümer Z, et al. Among authors: horn n. Hum Mol Genet. 1992 Oct;1(7):483-9. doi: 10.1093/hmg/1.7.483. Hum Mol Genet. 1992. PMID: 1307248

3

Menkes disease: an X-linked neurological disorder of the copper metabolism.

Horn N, Tønnesen T, Tümer Z. Horn N, et al. Brain Pathol. 1992 Oct;2(4):351-62. doi: 10.1111/j.1750-3639.1992.tb00711.x. Brain Pathol. 1992. PMID: 1341968 Review.

4

Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2.

Tümer Z, Tommerup N, Tønnesen T, Kreuder J, Craig IW, Horn N. Tümer Z, et al. Among authors: horn n. Hum Genet. 1992 Mar;88(6):668-72. doi: 10.1007/BF02265295. Hum Genet. 1992. PMID: 1348049

5

Multipoint linkage analysis in Menkes disease.

Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N. Tønnesen T, et al. Among authors: horn n. Am J Hum Genet. 1992 May;50(5):1012-7. Am J Hum Genet. 1992. PMID: 1570830 Free PMC article.

6

Incidence of Menkes disease.

Tønnesen T, Kleijer WJ, Horn N. Tønnesen T, et al. Among authors: horn n. Hum Genet. 1991 Feb;86(4):408-10. doi: 10.1007/BF00201846. Hum Genet. 1991. PMID: 1999344

7

Clinical expression of Menkes syndrome in females.

Gerdes AM, Tønnesen T, Horn N, Grisar T, Marg W, Müller A, Reinsch R, Barton NW, Guiraud P, Joannard A, et al. Gerdes AM, et al. Among authors: horn n. Clin Genet. 1990 Dec;38(6):452-9. doi: 10.1111/j.1399-0004.1990.tb03612.x. Clin Genet. 1990. PMID: 2289318

8

Prenatal and postnatal diagnosis of Menkes disease, an inherited disorder of copper metabolism.

Tønnesen T, Horn N. Tønnesen T, et al. Among authors: horn n. J Inherit Metab Dis. 1989;12 Suppl 1:207-14. doi: 10.1007/BF01799296. J Inherit Metab Dis. 1989. PMID: 2509808

9

[Has Menckes' disease disappeared? Clinical picture and postnatal diagnosis].

Tønnesen T, Gerdes AM, Horn N. Tønnesen T, et al. Among authors: horn n. Ugeskr Laeger. 1989 Nov 6;151(45):2975-7. Ugeskr Laeger. 1989. PMID: 2588391 Danish.

10

First-trimester diagnosis of Menkes disease: intermediate copper values in chorionic villi from three affected male fetuses.

Tønnesen T, Gerdes AM, Damsgaard E, Miny P, Holzgreve W, Søndergaard F, Horn N. Tønnesen T, et al. Among authors: horn n. Prenat Diagn. 1989 Mar;9(3):159-65. doi: 10.1002/pd.1970090303. Prenat Diagn. 1989. PMID: 2710742

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