P. Møller

发表

Atrioventricular conduction time ‐a heritable trait?

A. Heiberg, P. Møller, Arvid Heiberg, 1980, Clinical genetics.

Family studies in Bechterew's syndrome (ankylosing spondylitis) III. Genetics

P. Møller, K. Berg, 1983, Clinical genetics.

Familial cardiomyopathy: Autosomally, dominantiy inherited congestive cardiomyopathy with two cases of septal hypertrophy in one family

S. Nitter‐Hauge, T. Hovig, P. Lunde, 1979, Clinical genetics.

Prenatal diagnosis of glycerol‐kinase deficiency associated with a DNA deletion on the short arm of the X‐chromosome

O. Søvik, K. Berg, C. Hellerud, 1987, Clinical genetics.

HLA antigens, psoriasis and acute anterior uveitis in Bechterew's syndrome (ankylosing spondylitis)

O. Vinje, P. Møller, K. Berg, 1982, Clinical genetics.

HLA Phenotypes and joint affection in psoriasis, acute anterior uveitis and chronic prostatitis

K. Berg, O. Vinje, P. Møller, 1981, Clinical genetics.

Pi phenotypes in patients with ankylosing spondylitis, acute anterior uveitis, psoriasis and chronic prostatitis

M. Fagerhol, P. Møller, P. Møller, 1984, Clinical genetics.

The distribution of clinical findings in Bechterew's syndrome (ankylosing spondylitis) suggests distinct genetic subgroups

K. Berg, O. Vinje, P. Møller, 1982, Clinical genetics.

HLA A antigens in HLA 627 positive acute anterior uveitis

K. Berg, P. Møller, 1983, Clinical genetics.

Linkage disequilibrium analyses and restriction mapping of four RFLPs at the proα2(I) collagen locus: lack of correlation between linkage disequilibrium and physical distance

A. Børresen, K. Berg, P. Møller, 1988, Human Genetics.

Prenatal diagnosis in a female carrying a deletion close to the duchenne locus

H. Boman, P. Møller, K. Berg, 1988, Prenatal diagnosis.

Evidence for a sperm mutation resulting in Duchenne muscular dystrophy

A. Børresen, A. Heiberg, P. Møller, 1987, Clinical genetics.

Spinal muscular atrophy type I combined with atrial septal defect in three sibs

K. Skullerud, S. Nitter‐Hauge, A. Børresen, 1990, Clinical genetics.

The atrioventricular conduction time ‐ a heritable trait?: III Twin studies

K. Berg, A. Heiberg, P. Møller, 1982, Clinical genetics.

Unexpected findings at prenatal diagnosis

K. Berg, E. Ormerod, P. Møller, 1984 .

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)

P. Møller, G. Capellá, J. Mecklin, 2007, Journal of Medical Genetics.

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)

G. Capellá, C. Engel, J. Burn, 2007, Journal of Medical Genetics.