J. Mohr

发表

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

M. Bisgaard, K. Fenger, S. Bülow, 1994, Human mutation.

Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic Dna Marker Author(s): Lap

L. Tsui, N. Plavsic, H. Eiberg, 2022 .

Batten disease (Spielmeyer‐Sjogren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16

H. Eiberg, J. Mohr, R. Gardiner, 1989, Clinical genetics.

Concerning the Genetics of Mental Features

J. Mohr, 1962 .

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

H. Eiberg, J. Mohr, C. Hansen, 2005, American journal of medical genetics. Part A.

Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin

T. Rosenberg, H. Eiberg, J. Mohr, 1988, Clinical genetics.

Linkage relationships of paraoxonase (PON) with other markers: indication of PON‐cystic fibrosis synteny

H. Eiberg, R. Williamson, J. Mohr, 1985, Clinical genetics.

Number of “high genes” involved in determining the activity of paraoxonase

H. Eiberg, K. Fenger, J. Mohr, 1986, Clinical genetics.

Major locus for red hair color linked to MNS blood groups on chromosome 4

H. Eiberg, J. Mohr, Hans Eiberg, 1987, Clinical genetics.

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

H. Eiberg, J. Mohr, 1996, Human Genetics.

Linkage between the loci for cystic fibrosis and paraoxonase

L. Tsui, W. Warwick, H. Eiberg, 1986, Clinical genetics.

Genetics of paraoxonase

H. Eiberg, J. Mohr, 1981, Annals of human genetics.

CHROMOSOMAL ABERRATION AND MALFORMATIONS

J. Mohr, 1968, Acta ophthalmologica.

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

H. Eiberg, J. Mohr, L. Nielsen, 1986, Clinical genetics.

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

J. Mohr, H. Elberg, 1987, Clinical genetics.

Seasonal variation in the birth of children with aneuploid chromosome abnormalities

G. B. Petersen, J. Philip, N. Skakkebæk, 1973, Humangenetik.

Seasonal variation in the birth of children with aneuploid chromosome abnormalities. Report from the Danish Cytogenetic Central Register.

G. B. Petersen, J. Philip, N. Skakkebæk, 1973 .

Linkage between serum cholinesterase 2 (CHE2) and γ‐crystallin gene cluster (CRYG): assignment to chromosome 2

H. Eiberg, J. Mohr, M. Bisgaard, 1989, Clinical genetics.

Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q

H. Eiberg, J. Mohr, I. Berendt, 1995, Nature Genetics.

An example of rapid prenatal diagnosis of Fabry's disease usingmicrotechniques

H. Galjaard, J. Mohr, S. Sørensen, 1974, Clinical genetics.

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

R. Fodde, J. Mohr, J. Kleibeuker, 1996, Gastroenterology.

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

H. Eiberg, J. Mohr, P. Conneally, 1987, Clinical genetics.

Assignment of Granular Corneal Dystrophy Groenouw Type I (CDGG1) to Chromosome 5q

H. Eiberg, J. Mohr, H. Møller, 1994, European journal of human genetics : EJHG.

Linkage of plasma α‐L‐fucosidase (FUCA2) and the plasminogen (PLG) system

H. Eiberg, J. Mohr, L. Nielsen, 1984 .

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

H. Eiberg, J. Mohr, L. Nielsen, 1984, Clinical genetics.

Assignment of Genes Coding for Brown Eye Colour (BEY2) and Brown Hair Colour (HCL3) on Chromosome 15q

H. Eiberg, J. Mohr, 1996, European journal of human genetics : EJHG.

An MHC (HLA-A, -B, C2, BF, HLA-DR, GLO1) haplotype study of 497 Danish normal families with 1970 children including 97 twin pairs.

H. Eiberg, K. Fenger, J. Mohr, 1990, Tissue antigens.

Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

J. Mohr, K. B. Nielsen, F. Egede, 1979, Journal of medical genetics.

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

H. Eiberg, J. Mohr, 1977, Clinical genetics.

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

H. Eiberg, E. Niebuhr, J. Mohr, 1987, Clinical genetics.

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

A. Cats, R. Fodde, R. Kolodner, 1996, American journal of human genetics.

Δ‐Aminolevulinatedehydrase: synteny with ABO‐AK1‐ORM (and assignment to chromosome 9)

H. Eiberg, J. Mohr, L. Nielsen, 1983, Clinical genetics.

The establishment of an HNPCC register.

S. Bülow, J. Mohr, I. Bernstein, 1994, Anticancer research.

Mapping status of cystic fibrosis

H. Eiberg, J. Mohr, K. Schmiegelow, 1986 .

Number of loci responsible for the inheritance of high and low activity of paraoxonase

H. Eiberg, J. Mohr, A. Nielsen, 1986, Clinical genetics.

Cystic fibrosis; hint of linkage with F13B

H. Eiberg, E. Niebuhr, J. Mohr, 1985, Clinical Genetics.