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Showing 1 - 3 results of 3 for search 'Weinreich Stephanie', query time: 0.06s Refine Results
  1. 1
    Raising awareness of carrier testing for hereditary haemoglobinopathies in high-risk ethnic groups in the Netherlands: a pilot study among the general public and primary care providers
    Raising awareness of carrier testing for hereditary haemoglobinopathies in high-risk ethnic groups in the Netherlands: a pilot study among the general public and primary care provi...
    by Cornel Martina C, Rijmen Frank, de Lange-de Klerk Elly SM, Weinreich Stephanie S, de Kinderen Marja, Plass Anne
    Published 2009-09-01
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    Article
  2. 2
    Public support for neonatal screening for Pompe disease, a broad-phenotype condition
    Public support for neonatal screening for Pompe disease, a broad-phenotype condition
    by Weinreich Stephanie, Rigter Tessel, van El Carla, Dondorp Wybo, Kostense Pieter, van der Ploeg Ans T, Reuser Arnold JJ, Cornel Martina, Hagemans Marloes
    Published 2012-03-01
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    Article
  3. 3
    From rationing to rationality: an n-of-one trial service for off-label medicines for rare (neuromuscular) diseases
    From rationing to rationality: an n-of-one trial service for off-label medicines for rare (neuromuscular) diseases
    by Weinreich Stephanie S, Vrinten Charlotte, Verschuuren Jan JGM, Uyl-de Groot Carin A, Kuijpers Marja R, Sterrenburg Ellen, Scholten Rob JPM, van Bezooijen Cees FRM, Timmen Marcel FTH, van Weely Sonja, Cornel Martina C
    Published 2012-11-01
    Article
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