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Search Results - Nielsen, Inge-Merete
Search Results - Nielsen, Inge-Merete
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Abdominal Wall Defects in Greenland 1989–2015
by
Bugge, Merete
,
Drachmann, Gitte
,
Kern, Peder
,
Budtz–Jørgensen, Esben
,
Eiberg, Hans
,
Olsen, Britta
,
Tommerup, Niels
,
Nielsen, Inge‐Merete
Published in
Birth defects research
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A missense mutation in FIC1 is associated with greenland familial cholestasis
by
Klomp, Leo W.J.
,
Bull, Laura N.
,
Knisely, Alexander S.
,
van der Doelen, Marjolein A.M.
,
Juijn, Jenneke A.
,
Berger, Ruud
,
Forget, Sylviane
,
Nielsen, Inge-Merete
,
Eiberg, Hans
,
Houwen, Roderick H.J.
Published in
Hepatology (Baltimore, Md.)
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A high frequent BRCA1 founder mutation identified in the Greenlandic population
by
Harboe, Theresa Larriba
,
Eiberg, Hans
,
Kern, Peder
,
Ejlertsen, Bent
,
Nedergaard, Lotte
,
Timmermans-Wielenga, Vera
,
Nielsen, Inge-Merete
,
Bisgaard, Marie Luise
Published in
Familial cancer
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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland
by
Homøe, Preben
,
Koch, Anders
,
Rendtorff, Nanna Dahl
,
Lodahl, Marianne
,
Andersen, Ture
,
Andersen, Stig
,
Eiberg, Hans
,
Nielsen, Inge-Merete
,
Tranebjærg, Lisbeth
Published in
International journal of audiology
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Linkage Studies of Cholestasis Familiaris Groenlandica/Byler-Like Disease with Polymorphic Protein and Blood Group Markers
by
Eiberg, Hans
,
Nielsen, Inge-Merete
Published in
Human heredity
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Six years prenatal screening for 2 lethal autosomal recessive inheritable diseases: cholestasis familiaris groenlandica and propionic acidemia
by
Nielsen, Inge-Merete
,
Kern, Peder
,
Bisgaard, Marie Luise
,
Eiberg, Hans
Published in
Circumpolar health supplements
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Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)
by
Eiberg, Hans
,
Hansen, Lars
,
Korbo, Lise
,
Nielsen, Inge-Merete
,
Svenstrup, Kirsten
,
Bech, Sara
,
Pinborg, Lars H
,
Hjermind, Lena E
,
Olsen, Ove R
,
Nielsen, Jørgen E
Published in
Circumpolar health supplements
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High Incidence of Propionic Acidemia in Greenland Is Due to a Prevalent Mutation, 1540insCCC, in the Gene for the β-Subunit of Propionyl CoA Carboxylase
by
Ravn, Kirstine
,
Chloupkova, Maja
,
Christensen, Ernst
,
Brandt, Niels Jacob
,
Simonsen, Henrik
,
Kraus, Jan P.
,
Nielsen, Inge Merete
,
Skovby, Flemming
,
Schwartz, Marianne
Published in
American journal of human genetics
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Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder
by
Nørby, S
,
Lestienne, P
,
Nelson, I
,
Nielsen, I M
,
Schmalbruch, H
,
Sjö, O
,
Warburg, M
Published in
Journal of medical genetics
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