Mohr J - Search Results

1

Assignment of genes coding for brown eye colour (BEY2) and brown hair colour (HCL3) on chromosome 15q.

Eiberg H, Mohr J. Eiberg H, et al. Among authors: mohr j. Eur J Hum Genet. 1996;4(4):237-41. doi: 10.1159/000472205. Eur J Hum Genet. 1996. PMID: 8875191

2

Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24-p21.2 and exclusion of beta-CATENIN and MLH1.

Eiberg H, Hansen L, Hansen C, Mohr J, Teglbjaerg PS, Kjaer KW. Eiberg H, et al. Among authors: mohr j. Am J Med Genet A. 2005 Feb 15;133A(1):44-7. doi: 10.1002/ajmg.a.30568. Am J Med Genet A. 2005. PMID: 15637721

3

delta-Aminolevulinatedehydrase: synteny with ABO-AK1-ORM (and assignment to chromosome 9).

Eiberg H, Mohr J, Nielsen LS. Eiberg H, et al. Among authors: mohr j. Clin Genet. 1983 Feb;23(2):150-4. doi: 10.1111/j.1399-0004.1983.tb01864.x. Clin Genet. 1983. PMID: 6839527

4

Major genes of eye color and hair color linked to LU and SE.

Eiberg H, Mohr J. Eiberg H, et al. Among authors: mohr j. Clin Genet. 1987 Mar;31(3):186-91. doi: 10.1111/j.1399-0004.1987.tb02793.x. Clin Genet. 1987. PMID: 3568446

5

Dombrock blood group (DO): assignment to chromosome 12p.

Eiberg H, Mohr J. Eiberg H, et al. Among authors: mohr j. Hum Genet. 1996 Nov;98(5):518-21. doi: 10.1007/s004390050251. Hum Genet. 1996. PMID: 8882867

6

Linkage of plasma alpha-L-fucosidase (FUCA2) and the plasminogen (PLG) system.

Eiberg H, Mohr J, Nielsen LS. Eiberg H, et al. Among authors: mohr j. Clin Genet. 1984 Jul;26(1):23-9. doi: 10.1111/j.1399-0004.1984.tb00782.x. Clin Genet. 1984. PMID: 6590153

7

Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.

Bisgaard ML, Eiberg H, Møller N, Niebuhr E, Mohr J. Bisgaard ML, et al. Among authors: mohr j. Clin Genet. 1987 Aug;32(2):118-9. doi: 10.1111/j.1399-0004.1987.tb03337.x. Clin Genet. 1987. PMID: 3652490

8

Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22.

Eiberg H, Møller N, Mohr J, Nielsen LS. Eiberg H, et al. Among authors: mohr j. Clin Genet. 1986 May;29(5):354-9. doi: 10.1111/j.1399-0004.1986.tb00504.x. Clin Genet. 1986. PMID: 3461892

9

Colton blood groups: indication of linkage with the Kidd (Jk) system as support for assignment to chromosome 7.

Mohr J, Eiberg H. Mohr J, et al. Clin Genet. 1977 May;11(5):372-4. doi: 10.1111/j.1399-0004.1977.tb01329.x. Clin Genet. 1977. PMID: 862214

10

Assignment of granular corneal dystrophy Groenouw type I (CDGG1) to chromosome 5q.

Eiberg H, Møller HU, Berendt I, Mohr J. Eiberg H, et al. Among authors: mohr j. Eur J Hum Genet. 1994;2(2):132-8. doi: 10.1159/000472353. Eur J Hum Genet. 1994. PMID: 8044658

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

Search Page

Search Results