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Search works, persons, organizations and subjects:
perinnöllisyystiede
URI:
http://www.yso.fi/onto/yso/p5147
name
perinnöllisyystiede
Works about perinnöllisyystiede
Aspects on the management of salivary gland mucoepidermoid carcinoma in Finland
Bioinformatic approaches for integration of genomic information
Bioinformatic tools for analysis, mining and modelling large-scale gene expression and drug testing datasets
Composition and cryopreservation of sperm from some Finnish freshwater teleost fish
Consequences of balanced translocations and loss-of-function mutations
Conservation genetics of the Saimaa ringed seal :
Differential functions of mammalian Cdk7 and CCRK kinases in regulating transcription and ciliogenesis
Elämän tiede : tutkimus lääketieteellisestä teknologiasta, vanhemmuudesta ja perimän hallinnasta
Fatty acid metabolism genes LDLR, SOAT1 and DHCR24 and Alzheimer's disease risk
FGF signaling in neurogenesis and patterning of the developing midbrain and anterior hindbrain
Finland : the making of a nation : an attempt at an ethnic history of Finland
FISH mapping : from chromosomal localization to an ESTablished transcript map
Functional characterization of MutS homologue mismatch repair proteins and their variants
GATA factors regulate inner ear development and midbrain neurogenesis
Geeni, yksilö ja laji : tutkielmia perinnöllisyystieteen alalta
Geneettiset algoritmit : Genetic algorithms
Genetic epidemiology of hereditary prostate cancer in Finland
Genetic structure of Atlantic salmon in the Baltic Sea, stock mixture analysis and conservation strategies
Genetic studies on primary immunodeficiency diseases
Genetic studies on susceptibility genes in osteoarthritis
Genetic susceptibility to asbestos and tobacco smoke related non-malignant pleuropulmonary changes
Genetic variants predisposing to cardiac arrhythmia disorders and sudden cardiac death
Genetics and genomics of musical abilities
Genetics of inherited dementing disorders : special emphasis on Alzheimer's disease, frontotemporal dementia, Parkinson's disease and primary familial brain calcification
Genetics of obesity : abstracts
Genetics of rheumatoid arthritis : HLA, familiality and gender
Genetics, negotiated ethics and the ambiguities of moral choices
Genetiikkaa sukututkijoille ja väestöjen juurtenetsijöille
Genome-wide associations and computational search for the genetic risk factors for diabetic nephropathy
Haasteena harvinaiset harmit : Väestöliiton perinnöllisyysklinikka 20 vuotta
Homo europaeus : eurooppalaisen ihmisen pitkä historia
Human genetic variation in the Baltic Sea region : features of population history and natural selection
Idiopathic normal pressure hydrocephalus :
In quest of genetic susceptibility to disorders manifesting in fractures : assessing the significance of genetic factors in femoral neck stress fractures and childhood non-OI primary osteoporosis
Investigating the genetic susceptibility to rare and common manifestations
Johdatus geneettiseen sukututkimukseen
Juuresi näkyvät : geneettisen sukututkimuksen ABC
Kansamme parhaaksi : rotuhygienia Suomessa vuoden 1935 sterilointilakiin asti
Kliinisen mikrobiologian ja genetiikan tutkimukset
Kärpänen, hiiri ja ihminen
Large-scale data analysis to identify novel disease phenotypes and genes
Lipopolysaccharide : a link between periodontitis and cardiometabolic disorders
Lyhyt selitys pienille ja isoille asioille molekyyleistä mustiin aukkoihin
Me ja ne : rotuopeista sukulaisuuteen
Metaproteomics of the human intestinal tract to assess microbial functionality and interactions with the host
Microbial identification by detection of ligation probes on DNA microarray
Mielenterveys uusiutuvana voimavarana
Mitochondrial medicine
Ne geenit! Ne geenit!
Physiological adaptation to nutrient starvation : a key role for ERK7 in regulation of insulin secretion and metabolic homeostasis
Restrictions in the proliferative potential of inner ear hair cells and supporting cells
Samfundet Folkhälsans Genetiska institut 50 år
Sata vuotta perinnöllisyystiedettä Suomessa
Stress response of group I and II Clostridium botulinum
Studies on the molecular pathogenesis of neuronal ceroid lipofuscinoses in the animal models of CLN8 and CLN10
The 13th Rodens et Spatium Conference : abstracts
The CLN5 disease : protein maturation, trafficking and pathology
The DISC1 pathway in the genetic etiology of schizophrenia
The extended MHC haplotypes and their role in Sarcoidosis
The genetics of pubertal growth and timing
The role of The Peutz-Jeghers syndrome gene in hereditary and sporadic tumorigenesis
The search for susceptibility genes in lumbar disc degeneration : focus on young individuals
The spectrum of the phenotypes in the C9ORF72 expansion carriers : insights at the interface between neurology and psychiatry
Tiede ja elämä : tieteen päivät 2001
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