Horn N - Search Results

1

Molecular diagnosis of Menkes disease: genotype-phenotype correlation.

Møller LB, Mogensen M, Horn N. Møller LB, et al. Among authors: horn n. Biochimie. 2009 Oct;91(10):1273-7. doi: 10.1016/j.biochi.2009.05.011. Epub 2009 Jun 6. Biochimie. 2009. PMID: 19501626 Review.

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

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.

5

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

6

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

7

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

8

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

9

Variability in clinical expression of Menkes syndrome.

Gerdes AM, Tønnesen T, Pergament E, Sander C, Baerlocher KE, Wartha R, Güttler F, Horn N. Gerdes AM, et al. Among authors: horn n. Eur J Pediatr. 1988 Nov;148(2):132-5. doi: 10.1007/BF00445920. Eur J Pediatr. 1988. PMID: 3234433

10

Postmortem Menkes diagnosis from carrier testing of female relatives.

Tønnesen T, Silengo M, Gerdes AM, Hansen JC, Reske-Nielsen E, Franceschini P, Horn N. Tønnesen T, et al. Among authors: horn n. Clin Genet. 1987 Dec;32(6):393-7. doi: 10.1111/j.1399-0004.1987.tb03156.x. Clin Genet. 1987. PMID: 3436089

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