Schwartz M - Search Results

1

Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV.

Saillard J, Magalhães PJ, Schwartz M, Rosenberg T, Nørby S. Saillard J, et al. Among authors: schwartz m. Hum Biol. 2000 Dec;72(6):1065-8. Hum Biol. 2000. PMID: 11236862

2

Prevalence and Genetics of Leber Hereditary Optic Neuropathy in the Danish Population.

Rosenberg T, Nørby S, Schwartz M, Saillard J, Magalhães PJ, Leroy D, Kann EC, Duno M. Rosenberg T, et al. Among authors: schwartz m. Invest Ophthalmol Vis Sci. 2016 Mar;57(3):1370-5. doi: 10.1167/iovs.15-18306. Invest Ophthalmol Vis Sci. 2016. PMID: 27007794

3

An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.

Ravn K, Wibrand F, Hansen FJ, Horn N, Rosenberg T, Schwartz M. Ravn K, et al. Among authors: schwartz m. Eur J Hum Genet. 2001 Oct;9(10):805-9. doi: 10.1038/sj.ejhg.5200712. Eur J Hum Genet. 2001. PMID: 11781695

4

Aland eye disease: linkage data.

Schwartz M, Rosenberg T. Schwartz M, et al. Genomics. 1991 Jun;10(2):327-32. doi: 10.1016/0888-7543(91)90315-6. Genomics. 1991. PMID: 2071141

5

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.

Schwartz M, Yang HM, Niebuhr E, Rosenberg T, Page DC. Schwartz M, et al. Hum Genet. 1988 Feb;78(2):156-60. doi: 10.1007/BF00278188. Hum Genet. 1988. PMID: 3422216

6

Identification of mutations in Danish choroideremia families.

Schwartz M, Rosenberg T, van den Hurk JA, van de Pol DJ, Cremers FP. Schwartz M, et al. Hum Mutat. 1993;2(1):43-7. doi: 10.1002/humu.1380020108. Hum Mutat. 1993. PMID: 8477262

7

Prenatal diagnosis of choroideremia.

Schwartz M, Rosenberg T. Schwartz M, et al. Acta Ophthalmol Scand Suppl. 1996;(219):33-6. doi: 10.1111/j.1600-0420.1996.tb00381.x. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741114

8

X-linked ocular albinism: prevalence and mutations--a national study.

Rosenberg T, Schwartz M. Rosenberg T, et al. Among authors: schwartz m. Eur J Hum Genet. 1998 Nov-Dec;6(6):570-7. doi: 10.1038/sj.ejhg.5200226. Eur J Hum Genet. 1998. PMID: 9887374

9

A deletion panel of the long arm of the X chromosome: subregional localization of 22 DNA probes.

Yang HM, Lund T, Niebuhr E, Nørby S, Schwartz M, Shen L. Yang HM, et al. Among authors: schwartz m. Hum Genet. 1990 Jun;85(1):25-30. doi: 10.1007/BF00276321. Hum Genet. 1990. PMID: 1972695

10

Age differences of visual field impairment and mutation spectrum in Danish choroideremia patients.

Rosenberg T, Schwartz M. Rosenberg T, et al. Among authors: schwartz m. Acta Ophthalmol (Copenh). 1994 Dec;72(6):678-82. doi: 10.1111/j.1755-3768.1994.tb04679.x. Acta Ophthalmol (Copenh). 1994. PMID: 7747574

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

6,296 results

Search Page

Filters