Hasil Pencarian - Grigorescu-Sido Paula

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  1. 1
    GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss

    GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss oleh Lazăr Călin, Popp Radu, Al-Khzouz Camelia, Mihuț Gheorghe, Grigorescu-Sido Paula

    Diterbitkan 2017-03-01
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  2. 2
    Laboratory diagnosis and follow-up of Romanian Gaucher disease patients

    Laboratory diagnosis and follow-up of Romanian Gaucher disease patients oleh Drugan Cristina, Drugan Tudor, Caillaud Catherine, Grigorescu-Sido Paula, Nistor Tiberiu, Crăciun Alexandra M.

    Diterbitkan 2017-07-01
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  3. 3
    Mucopolysaccharidosis type I - Clinical and genetic characteristics of Romanian patients

    Mucopolysaccharidosis type I - Clinical and genetic characteristics of Romanian patients oleh Alkhzouz Camelia, Lazea Cecilia, Miclea Diana, Asavoaie Carmen, Nascu Ioana, Pop Tudor, Grigorescu-Sido Paula

    Diterbitkan 2020-07-01
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  4. 4
    Evaluation of c677t and a1298c polymorphism of the methylenetetrahydrofolate reductase gene as a maternal risk factor for trisomy 21 (a monocentric study)

    Evaluation of c677t and a1298c polymorphism of the methylenetetrahydrofolate reductase gene as a maternal risk factor for trisomy 21 (a monocentric study) oleh Bucerzan Simona, Popp Radu Anghel, Vlad Raluca Maria, Lazea Cecilia, Nicolaescu Radu, Grigorescu-Sido Paula

    Diterbitkan 2017-03-01
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