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Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a...
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Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1 :phenotype...
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Systematic family screening for familial hypercholesterolemia in Iceland
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Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by...
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Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with c...
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Mutations in MKKS cause obesity, retinal dystrophy and renal malformations assoc...
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Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation o...
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Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular...
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Clinical features and genotype of adenine phosphoribosyltransferase deficiency i...
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BRCA2 mutation in Icelandic prostate cancer patients
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Missense mutations causing mild hemophilia A in Iceland detected by denaturing g...
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A molecular survey of phenylketonuria in Iceland: identification of a founding m...
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Polymorphism of PRNP codons in the normal Icelandic population.
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Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by...
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Possible association of a cholecystokinin promotor polymorphism (CCK-36CT) with...
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Notkun ensímhvattrar fjölföldunar á DNA til að skima eftir erfðagalla í apóprótí...
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Establishment of three human breast epithelial cell lines derived from carriers...
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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in...
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Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmoge...
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Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequ...
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21
Text
1
Author
Green, JS
3
Beales, PL
2
Davidson, WS
2
Katsanis, N
2
Lupski, JR
2
Parfrey, PS
2
Aaltonen, L A
1
Agnarsson, B A
1
Akama, T O
1
Ala-Kokko, L
1
Albrechtsen, Anders
1
Amartino, Hernan
1
Andersen, Stig
1
Andersen, Ture
1
Ansley, SJ
1
Arason, A
1
Arnason, A
1
Asselbergs, Folkert W
1
Backenhorn, K
1
Bao, W
1
Barkardottir, R B
1
Batbayli, Mustafa
1
Benediktsdottir, K
1
Bergsten, Eva Boje
1
Bermúdez-Jiménez, Francisco
1
Bertini, Enrico
1
Bianchi, Marzia
1
Bjornsson, A
1
Bjornsson, Johannes
1
Borg, A
1
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Topic
DNA Mutational Analysis
Female
18
Humans
18
Male
17
Adult
12
Middle Aged
11
Iceland
10
Pedigree
10
Mutation
9
DNA
8
Adolescent
7
Aged
7
Genetic Predisposition to Disease
6
Polymorphism
6
Base Sequence
5
Child
5
Codon
5
Gene Frequency
5
Genotype
5
Haplotypes
5
Phenotype
5
Preschool
5
Amino Acid Sequence
4
Chromosome Mapping
4
Genetic
4
Point Mutation
4
Risk Factors
4
Bardet-Biedl Syndrome
3
Breast Neoplasms
3
Case-Control Studies
3
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Content Provider
Hirsla - Landspítali University Hospital research archive
12
University College London: UCL Discovery
3
University of Copenhagen: Research
3
Aarhus University: Research
1
Lehigh Valley Health Network: LVHN Scholarly Works
1
Sistema Sanitario Público de Andalucía (SSPA): Repositorio
1
Utrecht University Repository
1
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Greenland
2
Newfoundland
2
Norway
2
Arctic
1
Canada
1
Faroe Islands
1
Indian
1
Long Arm
1
Smella
1
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Language
English
19
unknown
2
Icelandic
1
Open Polar Keyword
Iceland
13
Newfoundland
4
Faroe Islands
2
Greenland
2
inuit
2
inuits
2
Arctic
1
East Greenland
1
Northern Finland
1
greenlandic
1
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