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Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a...
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Macular corneal dystrophy types I and II are caused by distinct mutations in the...
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Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic m...
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Large-scale whole-genome sequencing of the Icelandic population
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Mutations in MKKS cause obesity, retinal dystrophy and renal malformations assoc...
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Large-scale whole-genome sequencing of the Icelandic population.
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A molecular survey of phenylketonuria in Iceland: identification of a founding m...
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Article in Journal/Newspaper
7
Author
Arnar, David O
2
Besenbacher, Soren
2
Bjornsdottir, Gyda
2
Bjornsson, Einar S
2
Eyjolfsson, Gudmundur I
2
Frigge, Michael L
2
Gretarsdottir, Solveig
2
Gudbjartsson, Daniel F
2
Gudbjartsson, Hakon
2
Gudjonsson, Sigurjon A
2
Gudmundsdottir, Thora S
2
Gylfason, Arnaldur
2
Halldorsson, Bjarni V
2
Helgadottir, Hafdis Th
2
Helgason, Agnar
2
Helgason, Hannes
2
Hjartarson, Eirikur
2
Holm, Hilma
2
Johannsdottir, Hrefna
2
Jonasson, Jon G
2
Jonsson, Jon J
2
Kong, Augustine
2
Ludvigsson, Petur
2
Magnusson, Gisli
2
Magnusson, Olafur Th
2
Masson, Gisli
2
Oddson, Asmundur
2
Olafsson, Isleifur
2
Olafsson, Sigurdur
2
Rafnar, Thorunn
2
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Topic
Frameshift Mutation
Humans
7
Female
6
Iceland
5
DNA
4
Male
4
Pedigree
4
DNA Mutational Analysis
3
Gene Frequency
3
Genetic Predisposition to Disease
3
Middle Aged
3
Polymorphism
3
Sequence Analysis
3
80 and over
2
Aged
2
Atrial Fibrillation
2
Base Sequence
2
Bulbar Palsy
2
Founder Effect
2
G-Protein-Coupled
2
GTP-Binding Protein alpha Subunits
2
Genome
2
Genome-Wide Association Study
2
Genotype
2
Gs
2
Haplotypes
2
Hearing Loss
2
Homozygote
2
Human
2
INDEL Mutation
2
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Content Provider
Hirsla - LandspĂtali University Hospital research archive
4
Aarhus University: Research
1
University College London: UCL Discovery
1
University of Copenhagen: Research
1
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Geographic location
Indel’
2
Greenland
1
Norway
1
Language
English
7
Open Polar Keyword
Iceland
5
Greenland
1
Newfoundland
1
greenlandic
1
inuit
1
inuits
1
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