COLTON BLOOD GROUPS: INDICATION OF LINKAGE WITH THE KIDD (JK) SYSTEM AS SUPPORT FOR ASSIGNMENT TO CHROMOSOME 7.MOHR J; EIBERG H.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 5; PP. 372-374; BIBL. 4 REF.Article

DETERMINATION OF COMMON HAPTOGLOBIN PHENOTYPES IN EGYPTIANS AND DANES BY MEANS OF NON-CARCINOGENIC STAIN REAGENTSHABIB Z; EIBERG H.1983; HEREDITAS; ISSN 0018-0661; SWE; DA. 1983; VOL. 98; NO 2; PP. 219-223; BIBL. 38 REF.Article

GENETICS OF PARAOSCONASEEIBERG H; MOHR J.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; NO 4; PP. 323-330; BIBL. 8 REF.Article

DELTA -AMINOLEVULINATEDEHYDRASE: SYNTENY WITH ABO-AK1-ORM (AND ASSIGNMENT TO CHROMOSOME 9)EIBERG H; MOHR J; NIELSEN LS et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 2; PP. 150-154; BIBL. 5 REF.Article

NEONATAL AND MATERNAL LYMPHOCYTES IN WHOLE-BLOOD CULTURES: ABSENCE OF STRONG INTERACTIONEIBERG H; MOHR J; NIELSEN KR et al.1978; VOX SANG.; CHE; DA. 1978; VOL. 35; NO 5; PP. 288-293; BIBL. 7 REF.Article

Dombrock blood group (DO) : assignment to chromosome 12pEIBERG, H; MOHR, J.Human genetics. 1996, Vol 98, Num 5, pp 518-521, issn 0340-6717Article

Linkage studies of cholestasis familiaris Groenlandica/Byler-like disease with polymorphic protein and blood group markersEIBERG, H; NIELSEN, I.-M.Human heredity. 1993, Vol 43, Num 4, pp 250-256, issn 0001-5652Article

Major locus for red hair color linked to MNS blood grups on chromosome 4EIBERG, H; MOHR, J.Clinical genetics. 1987, Vol 32, Num 2, pp 125-128, issn 0009-9163Article

Total genome scan analysis in a single extended family for primary nocturnal enuresis : Evidence for a new locus (ENUR3) for primary nocturnal enuresis on chromosome 22q11EIBERG, H.European urology. 1998, Vol 33, pp 34-36, issn 0302-2838, SUP3Conference Paper

Identity of the polymorphisms for esterase D and s-formylglutathione hydrolase in red blood cellsEIBERG, H; MOHR, J.Human genetics. 1986, Vol 74, Num 2, pp 174-175, issn 0340-6717Article

Major genes of eye color and hair Color linked to LU and SEEIBERG, H; MOHR, J.Clinical genetics. 1987, Vol 31, Num 3, pp 186-191, issn 0009-9163Article

Identity of the polymorphisms for esterase D and s-formylglutathione hydrolase in red blood cellsEIBERG, H; MOHR, J.Human genetics. 1986, Vol 74, Num 2, pp 174-175, issn 0340-6717Article

Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1q by a linkage studyEIBERG, H; DEN TANDT, W. R.Human genetics. 1997, Vol 101, Num 2, pp 205-207, issn 0340-6717Article

Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobinEIBERG, H; MARNER, E; ROSENBERG, T et al.Clinical genetics. 1988, Vol 34, Num 4, pp 272-275, issn 0009-9163Article

Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13qEIBERG, H; BERENDT, I; MOHR, J et al.Nature genetics. 1995, Vol 10, Num 3, pp 354-356, issn 1061-4036Article

Linkage of plasma α-L-fucosidase (FUCA2) and the plasminogen (PLG) systemEIBERG, H; MOHR, J; NIELSEN, L. S et al.Clinical genetics. 1984, Vol 26, Num 1, pp 23-29, issn 0009-9163Article

Heterogeneity of FeNO response to inhaled steroid in asthmatic childrenBUCHVALD, F; EIBERG, H; BISGAARD, H et al.Clinical and experimental allergy (Print). 2003, Vol 33, Num 12, pp 1735-1740, issn 0954-7894, 6 p.Article

Number of loci responsible for the inheritance of high and low activity of paraoxonaseNIELSEN, A; EIBERG, H; MOHR, J et al.Clinical genetics. 1986, Vol 29, Num 3, pp 216-221, issn 0009-9163Article

Number of «high genes» involved in determining the activity of paraoxonaseNIELSEN, A; EIBERG, H; FENGER, K et al.Clinical genetics. 1986, Vol 30, Num 1, pp 41-49, issn 0009-9163Article

Confirmation of F13A assignment and sequence information concerning F13A-HLA-GLOEIBERG, H; NIELSEN, L. S; MOHR, J et al.Clinical genetics. 1984, Vol 26, Num 5, pp 385-388, issn 0009-9163Article

Suggestion of linkage between manic-depressive illness and the enzyme phosphoglycolate phosphatase (PGP) on chromosome 16pEIBERG, H; EWALD, H; MORS, O et al.Clinical genetics. 1993, Vol 44, Num 5, pp 254-257, issn 0009-9163Article

Batten disease (Spielmeyer-Sjøgren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16EIBERG, H; GARDINER, R. M; MOHR, J et al.Clinical genetics. 1989, Vol 36, Num 4, pp 217-218, issn 0009-9163Article

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I: Linkage analysisEIBERG, H; KJER, B; KJER, P et al.Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 977-980, issn 0964-6906Article

Transferrin subtypes in 51 Danish patients with hereditary haemochromatosis and in 847 normal subjectsMILMAN, N; EIBERG, H; THYMANN, M et al.Human genetics. 1992, Vol 88, Num 4, pp 475-476, issn 0340-6717Article

Linkage between α₁B-glycoprotein (A1BG) and Lutheran (LU) red blood group system: assignment to chromosome 19: new genetic variants of A1BGEIBERG, H; BISGAARD, M. L; MOHR, J et al.Clinical genetics. 1989, Vol 36, Num 6, pp 415-418, issn 0009-9163Article