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Bothnia dystrophy, a clinical, genetical and electrophysiological study

by Burstedt, Marie
Published 2003

causing amyloid angiopathy and brain hemorrhage ‐ clinical genetics in Iceland

by Jensson, Olafur, Palsdottir, Astridur, Thorsteinsson, Leifur, Arnason, Alfred
Published in Clinical Genetics (1989)

Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy

by Ostergaard, Elsebet, Batbayli, Mustafa, Duno, Morten, Vilhelmsen, Kaj
Published in Journal of Medical Genetics (2010)

Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy

by Ostergaard, Elsebet, Batbayli, Mustafa, Duno, Morten, Vilhelmsen, Kaj
Published in Journal of Medical Genetics (2010)

Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy

Published in Journal of Medical Genetics (2011)

Genetic Loss of Sucrase-Isomaltase Function: Mechanisms, Implications, and Future Perspectives

by Senftleber,Ninna Karsbæk, Ramne,Stina, Moltke,Ida, Jørgensen,Marit Eika, Albrechtsen,Anders, Hansen,Torben, Andersen,Mette K
Published in The Application of Clinical Genetics (2023)

Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation

by Jensson, O, Stenbjerg Bernvil, S, Jonsdottir, S, Ingerslev, J
Published in Journal of Internal Medicine (2011)

Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation

by JENSSON, Ó., BERNVIL, S. STENBJERG, JÖNSÖDTTIR, S., INGERSLEV, J.
Published in Journal of Internal Medicine (1994)

Desafios para a universalização da genética clínica: o caso brasileiro Challenges for the universalization of clinical genetics: the Brazilian case

by Maria Concepción Novoa, Teresinha Fróes Burnham
Published 2011

Estimation of Newborn Risk for Child or Adolescent Obesity: Lessons from Longitudinal Birth Cohorts

by Morandi, Anita, Meyre, David, Lobbens, Stéphane, Kaakinen, Marika, Vatin, Vincent, Gaget, Stefan, Pouta, Anneli, Hartikainen, Anna-Liisa, Laitinen, Jaana, Ruokonen, Aimo, Das, Shikta, Khan, Anokhi Ali, Elliott, Paul, Maffeis, Claudio, Järvelin, Marjo-Riitta, Froguel, Philippe, Kleinman, Ken Paul, Rifas-Shiman, Sheryl Lynn, Gillman, Matthew William
Published in PLoS ONE (2012)

The Assent of a Nation: Genethics and Iceland

by McInnis, Melvin G.
Published in Clinical Genetics (1999)

Healthcare Burden in Greenland of Gastrointestinal Symptoms in Adults with Inherited Loss of Sucrase-Isomaltase Function

by Andersen, Kristine, Hansen, Torben, Jørgensen, Marit, Senftleber, Ninna
Published in The Application of Clinical Genetics (2024)

Population history and its impact on medical genetics in Quebec

by Laberge, A‐M, Michaud, J, Richter, A, Lemyre, E, Lambert, M, Brais, B, Mitchell, GA
Published in Clinical Genetics (2005)

The Vth Nordic Meeting of Medical Genetics: Laugarvatn, Iceland, August 27–28, 1988

Published in Clinical Genetics (1989)

Sjögren‐Larsson syndrome in Sweden: distribution of the gene

by Iselius, L., Jagell, S.
Published in Clinical Genetics (1989)

Molecular genetics of inherited retinal degenerations in Icelandic patients.

by Thorsteinsson, Daniel A, Stefansdottir, Vigdis, Eysteinsson, Thor, Thorisdottir, Sigridur, Jonsson, Jon J
Published in Clinical Genetics (2021)

Molecular genetics of inherited retinal degenerations in Icelandic patients

by Thorsteinsson, Daniel A., Stefánsdóttir, Vigdís Fjóla, Eysteinsson, Þór, Thorisdottir, Sigridur, Jónsson, Jón Jóhannes
Published in Clinical Genetics (2021)

Relation of mathematical ability to psychosis in Iceland

by Karlsson, Jon L
Published in Clinical Genetics (1999)

Serum esterases of Icelanders 1. A “silent” pseudocholinesterase gene in an icelandic family

by Arnason, Alfred, Jensson, Olafur, Gudmundsson, Sigurdur
Published in Clinical Genetics (1975)

The incidence of Down syndrome in northern Finland with special reference to maternal age

by Leisti, J., Vahtola, L., Linna, S.‐L., Herva, R., Koskela, S.‐L., Vitali, M.
Published in Clinical Genetics (1985)