173 research outputs found

    Some pioneers of European human genetics

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    Some of the pioneers of human genetics across Europe are described, based on a series of 100 recorded interviews made by the author. These interviews, and the memories of earlier workers in the field recalled by interviewees, provide a vivid picture, albeit incomplete, of the early years of human and medical genetics. From small beginnings in the immediate post-World War 2 years, human genetics grew rapidly across many European countries, a powerful factor being the development of human cytogenetics, stimulated by concerns over the risks of radiation exposure. Medical applications soon followed, with the recognition of human chromosome abnormalities, the need for genetic counselling, the possibility of prenatal diagnosis and later, the applications of human molecular genetics. The evolution of the field has been strongly influenced by the characters and interests of the relatively small number of founding workers in different European countries, as well as by wider social, medical and scientific factors in the individual countries

    Lionel Sharples Penrose, 1898-1972: A Personal Memoir in Celebration of the Centenary of His Birth

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    Prenatal diagnosis of genetic defects

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    Prenatal diagnosis of genetic defects

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    The Amish: Perceptions of Genetic Disorders and Services

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    http://dx.doi.org/10.1007/BF0142384

    The Neu-Laxova syndrome—a distinct entity

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