Mohr J - Search Results

1

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

Wijnen J, Khan PM, Vasen H, Menko F, van der Klift H, van den Broek M, van Leeuwen-Cornelisse I, Nagengast F, Meijers-Heijboer EJ, Lindhout D, Griffioen G, Cats A, Kleibeuker J, Varesco L, Bertario L, Bisgaard ML, Mohr J, Kolodner R, Fodde R. Wijnen J, et al. Among authors: mohr j. Am J Hum Genet. 1996 Feb;58(2):300-7. Am J Hum Genet. 1996. PMID: 8571956 Free PMC article.

2

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

Vasen HF, Wijnen JT, Menko FH, Kleibeuker JH, Taal BG, Griffioen G, Nagengast FM, Meijers-Heijboer EH, Bertario L, Varesco L, Bisgaard ML, Mohr J, Fodde R, Khan PM. Vasen HF, et al. Among authors: mohr j. Gastroenterology. 1996 Apr;110(4):1020-7. doi: 10.1053/gast.1996.v110.pm8612988. Gastroenterology. 1996. PMID: 8612988

3

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.

Bisgaard ML, Fenger K, Bülow S, Niebuhr E, Mohr J. Bisgaard ML, et al. Among authors: mohr j. Hum Mutat. 1994;3(2):121-5. doi: 10.1002/humu.1380030206. Hum Mutat. 1994. PMID: 8199592

4

Linkage between alpha 1B-glycoprotein (A1BG) and Lutheran (LU) red blood group system: assignment to chromosome 19: new genetic variants of A1BG.

Eiberg H, Bisgaard ML, Mohr J. Eiberg H, et al. Among authors: mohr j. Clin Genet. 1989 Dec;36(6):415-8. Clin Genet. 1989. PMID: 2591067

5

Linkage between serum cholinesterase 2 (CHE2) and gamma-crystallin gene cluster (CRYG): assignment to chromosome 2.

Eiberg H, Nielsen LS, Klausen J, Dahlén M, Kristensen M, Bisgaard ML, Møller N, Mohr J. Eiberg H, et al. Among authors: mohr j. Clin Genet. 1989 May;35(5):313-21. doi: 10.1111/j.1399-0004.1989.tb02951.x. Clin Genet. 1989. PMID: 2758686

6

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

7

The establishment of an HNPCC register.

Myrhøj T, Bernstein I, Bisgaard ML, Svendsen LB, Sondergaard JO, Mohr J, Dahl S, Bülow S. Myrhøj T, et al. Among authors: mohr j. Anticancer Res. 1994 Jul-Aug;14(4B):1647-50. Anticancer Res. 1994. PMID: 7979201

8

[Preclinical and prenatal diagnosis of familial adenomatous polyposis].

Bisgaard ML, Bülow S, Winther K, Eiberg H, Niebuhr E, Mohr J. Bisgaard ML, et al. Among authors: mohr j. Ugeskr Laeger. 1992 Mar 30;154(14):921-4. Ugeskr Laeger. 1992. PMID: 1315993 Danish.

9

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

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

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