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Linkage of cholestasis familiaris Groenlandica/Byler-like disease to chromosome...
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Abdominal Wall Defects in Greenland 1989–2015
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Abdominal Wall Defects in Greenland 1989–2015
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A high frequent BRCA1 founder mutation identified in the Greenlandic population
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Gastroschise og Omphalocele i Grønland 1989-2015
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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in...
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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in...
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GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in...
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A high frequent BRCA1 founder mutation identified in the Greenlandic population
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High Incidence of Propionic Acidemia in Greenland Is Due to a Prevalent Mutation...
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High Incidence of Propionic Acidemia in Greenland Is Due to a Prevalent Mutation...
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Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)
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A missense mutation in FIC1 is associated with greenland familial cholestasis
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A missense mutation in FIC1 is associated with greenland familial cholestasis
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A missense mutation in F1C1 is associated with Greenland familial cholestasis
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Genetics
Genetics (clinical)
Greenland
Adolescent
Adult
Aged
Audiometry
Bone Conduction
Cancer Research
Case-Control Studies
Child
Connexins
Cross-Sectional Studies
DNA Mutational Analysis
Female
Gene Frequency
Genetic Predisposition to Disease
Hearing
Hearing Impaired Persons
Hearing Loss
Hepatology
Heterozygote
Homozygote
Humans
Inuits
Language and Linguistics
Linguistics and Language
Male
Middle Aged
Mixed Conductive-Sensorineural
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