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Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose
Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation
Reports of Societies
Notes on Books
An Epitome of Current Medical Literature
HOSPITAL AND DISPENSARY MANAGEMENT
NOTES ON BOOKS
AN EPITOME OF CURRENT MEDICAL LITERATURE
THE BEGINNINGS OF THE CRIMINAL
Anti-pernicious Principle
Nova et Vetera
Medical News
Drug Assays on Organ Cultures of Biopsies from Human Tumours
Manifestation of hereditary fructose intolerance.
Prenatal Diagnosis of Galactosaemia
Endoscopic removal of a duodenal foreign body.
Current position of paternity tests.
Drunken driving among the young.
Biochemical neonatal screening.
Treatment of familial hypercholesterolaemia. United Kingdom lipid clinics study of pravastatin and cholestyramine.
Screening for cystic fibrosis Should begin with cascade screening
Human genome moves closer to reality
Survival in families with hereditary protein C deficiency, 1820 to 1993
Parkinson's disease genetics comes of age
Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study
Deaths attributed to haemochromatosis are rare in Britain
Getting closer to patients and their families
Genetic risk and behavioural change
Confidential inquiries should be funded in clinical genetics
Predictive genetics and predictive morphology have certain similarities
Longevity and C282Y mutation for haemochromatosis: Data do not support conclusion
BMA warns against unnecessary screening tests in private sector
Hypercholesterolaemia and its management
Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome
NGS identifies TAZ mutation in a family with X-linked dilated cardiomyopathy
Massive pulmonary embolism and thrombophilia
Presidential Address on the Relation of Pathology and Therapeutics to Clinical Medicine
Observations on the Etiology of Eczema
Reviews and Notices
The Complications and Sequelæ of Influenza
Reports and Analyses and Descriptions of New Inventions in Medicine, Surgery, Dietetics, and the Allied Sciences
Ireland
An Epitome of Current Medical Literature
India and the Colonies
A Clinical Lecture on Functional Nerve Diseases
The Causation of Cancer
PUERPERAL INSANITY
REVIEWS
MEDICO-PSYCHOLOGICAL ASSOCIATION OF GREAT BRITAIN AND IRELAND
New Zealand
An Address ON THE SO-CALLED FAMILY DISEASES: PREMATURE PHYSIOLOGICAL SENESCENCE LOCALIZED TO CERTAIN ORGANIC SYSTEMS
Letters, Notes, and Answers
AN EPITOME OF CURRENT MEDICAL LITERATURE
Address ON HEREDITY
Scotland
Reviews
Notes on Books
HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS
Reports of Societies
Reports of Societies
MATERNITY IN ITS SOCIOLOGICAL ASPECTS
Scotland
CRETINISM AND MYXOEDEMA
Respiratory Poisons
NATURE AND NURTURE: THE STUDY OF TWINS
Influence of Penicillin on Coagulation of Blood
Injuries Caused by Cold
Confluent Chicken-pox with Haemorrhagic Symptoms
SUPPLEMENT 2480
Galactose Diabetes
Questions and Comments
Clinical Aspects of Genetics
The geography of neurology.
Monoclonal theory of atheroma.
THE CENTENARY OF MENDEL'S DISCOVERY.
TGF-β1 genotype and accelerated decline in lung function of patients with cystic fibrosis
Home dampness, current allergic diseases, and respiratory infections among young adults
β2 adrenoceptor promoter polymorphisms: extended haplotypes and functional effects in peripheral blood mononuclear cells
Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry
Under recognition of late onset ornithine transcarbamylase deficiency
Epitome of Current Medical Literature
The Nature of Genius
Cystic Fibrosis and Fertility
Gross impairment of hepatic drug metabolism in a patient with chronic liver disease.
Treatment of seasonal and perennial rhinitis.
Treatment of erythema multiforme secondary to herpes simplex by prophylactic topical acyclovir.
Side of origin of epithelial ovarian cancer.
Genetic testing and insurance
Aspirin and pre-eclampsia
Biological influences on criminal behaviour: how good is the evidence?
An Ethical Debate: Testing may be unhelpful
Increased familial risk and evidence of genetic factor in migraine
Management of sickle cell disease
Polymorphism in high density lipoprotein paraoxonase gene and risk of acute myocardial infarction in men: prospective nested case-control study
Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study
Follow up after a family based genetic screening programme for familial hypercholesterolaemia: is screening alone enough?
Male subfertility
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