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dc.contributor.editorJones EM
dc.contributor.editorTansey EM
dc.date.accessioned2017-06-08T13:26:36Z
dc.date.available2017-06-08T13:26:36Z
dc.date.issued2014
dc.date.submitted2017-06-08T11:50:55.432Z
dc.identifier.isbn9780902238886
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/23669
dc.description.abstractChaired by Professor Martin Bobrow and introduced by Professor Bob Williamson, this Witness Seminar included geneticists from a broad range of research and clinical specialities. Discussions of molecular research into haemoglobin disorders, and the development of probes for related genes in the 1970s, included particular acknowledgment of Southern blotting as a critical tool for such research. Also noted was a landmark conference in Crete in 1978 that emphasized the special significance of research work on thalassaemia, as well as providing fruitful networking opportunities for scientists from around the world. Similarly, in 1982, a key course at Leiden University introduced molecular techniques to geneticists from across Europe. In that same year the first prenatal diagnosis by chorionic villus sampling was published, and the emotional aspects of such genetic diagnoses for patients, families and clinicians were frequently discussed during the seminar. Other issues, including the funding of research, and especially the role of patient support groups; the establishment and growth of professional interest groups and bodies such as the Clinical Molecular Genetics Society; and the development of national genetics.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesWellcome Witnesses to Contemporary Medicine;Volume 48
dc.subjectWellcome Witnesses to Contemporary Medicineen_US
dc.subjectHistory of Modern Biomedicine Research Groupen_US
dc.titleClinical Molecular Genetics in the UK c.1975–c.2000en_US
dc.typeBooken_US


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