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Search results
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CT findings of the temporal bone in CHARGE syndrome: aspects of importance in cochlear implant surgery
The course of clinically suspect arthralgia and early rheumatoid arthritis : clinical features, imaging and genetics
Employing biomarkers of healthy ageing for leveraging genetic studies into human longevity
Genetics and epigenetics of repeat derepression in human disease
A systematic review of interventions to provide genetics education for primary care
MYC transcription factors: masters in the regulation of jasmonate biosynthesis in Arabidopsis thaliana
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome
The importance of genetic diagnosis for Duchenne muscular dystrophy
Bioinformatic approaches to identify genomic, proteomic and metabolomic biomarkers for the metabolic syndrome
Immunogenetics of rheumatoid arthritis: Understanding functional implications
Molecular biomarkers predicting clinical outcome in colon and rectal cancer
IGSF1 variants in boys with familial delayed puberty
Candidate gene studies in rheumatoid arthritis
Genetics in juvenile idiopathic arthritis
Primary vascular tumours of bone: towards a new classification based on pathology and genetics
Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
Testing antidepressant compounds in a neuropsychological model of drug action
Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder
Genetics, statins, and lipid metabolism in cardiovascular disease
Bicuspid Aortic Valve Morphology and Associated Cardiovascular Abnormalities in Fetal Turner Syndrome: A Pathornorphological Study
Copy Number Variants in Short Children Born Small for Gestational Age
Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy
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