About: Clinical genetics

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Attributs	Valeurs
type	Concept
rdfs:label	Clinical genetics
skos:inScheme	http://hub.abes.fr/referentiel/hwpjournalcoll
is Subject of	MMR vaccine—worries are not justified Haemopoietic stem cell transplantation for genetic disorders ABC of clinical genetics. Treatment of genetic disorders. Innovation in the pharmaceutical industry MPs seek to control medical genetics Counsellors do not have to be genetic nurse specialists The everyday and the soon to be everyday Genealogy certainly matters for multifactorial genetic disease House of Lords supports human embryonic stem cell research Genetic risk and behavioural change Health benefits from genetics should be basic human right Breast screening guidelines should be adapted in Down's syndrome Survival after partial lung transplants is as good as after full lung transplants Clinical research under the cosh again HFEA widens its criteria for preimplantation genetic diagnosis The gene detective Hypercholesterolaemia and its management Choosing an antidepressant. Cystic fibrosis in adults. Is genetic information relevantly different from other kinds of non-genetic information in the life insurance context? Fas and Fas ligand expression in cystic fibrosis airway epithelium Aseptic rituals unmasked. NEWS AND NOTES A regional register for inherited cancers. News Building bodies Genetic testing and insurance End to insurers using genetic data urged Science, medicine, and the future: Molecular genetic approaches to understanding disease Netlines Scientists debate whether sperm counts are really falling Adding fatty acids to baby milk improves development Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases Human cells from cloned embryos in research and therapy France bans reproductive and therapeutic cloning US experts urge more neonatal screening for genetic disorders Folic acid, homocysteine, and cardiovascular disease: judging causality in the face of inconclusive trial evidence Communicating about screening MMR vaccine and autism Specialty services for children with special health care needs: supplement not supplant the medical home Presumed ataxia-telangiectasia in a man. Genetic engineering for medicine. ABC of clinical genetics. Special issues. ABC of clinical genetics. Gene structure and function. Minerva Retaining personal medical records of children who have had chemotherapy and radiotherapy Services for people with haemoglobinopathy Call for routine cystic fibrosis screening Screening for fragile X syndrome: a model for genetic disorders? Science, medicine, and the future : Gene therapy MMR vaccination and autism 1998 Arranging genes to create art and understanding Woman forced to have three embryos implanted is allowed fetal reduction to save her life Management of hypertrophic cardiomyopathy Andrew Wakefield is accused of paying children for blood samples Controversial embryo bill receives second hearing in Lords A man with congenital abnormalities and psychotic symptoms Somatic Mutation and Chronic Disease Acute gastroenteritis. Ascertainment and Prevention of Genetic Disease Social Effects of Genetic Counselling Cleaner medicaments. Medicine and Books How to commission a portrait Experience with screening newborns for Duchenne muscular dystrophy in Wales. News Fetal blood sampling in retreat. Statistical analysis inappropriate Autistic spectrum disorders Blood tests urged for CJD carriers Health insurance company offers genetic screening to its clients MP is criticised for saying that marriage of first cousins is a health problem Israeli Arabs undergo less preventive screening than Jews From small things Researchers create human sperm using embryonic stem cells Reviews Prolonged endotracheal intubation. Prenatal diagnosis of the haemoglobinopathies. Damaged laryngeal nerves in thyroid surgery. Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13 A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36 Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 No association between the EN2 gene and autistic disorder A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13 Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy Homozygosity mapping of a third Joubert syndrome locus to 6q23 Lamin A expression levels are unperturbed at the normal and mutant alleles but display partial splice site selection in Hutchinson-Gilford progeria syndrome Evidence for a gene influencing haematocrit on chromosome 6q23-24: genomewide scan in the Framingham Heart Study Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11 Homozygosity mapping to the USH2A locus in two isolated populations Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR Hirschsprung disease, associated syndromes, and genetics: a review Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM Peutz-Jeghers families unlinked toSTK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma Genome-wide linkage scan for plasma high density lipoprotein cholesterol, apolipoprotein A-1 and triglyceride variation among American Indian populations: the Strong Heart Family Study Genetic counselling.

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