Showing 1 - 3 results of 3 for search 'Egle Preiksaitiene', query time: 0.04s Refine Results
  1. 1
    A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability

    A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability by Živilė Maldžienė, Evelina M. Vaitėnienė, Beata Aleksiūnienė, Algirdas Utkus, Eglė Preikšaitienė

    Published 2020
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  2. 2
    Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement

    Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement by Egle Preiksaitiene, Eglė Benušienė, Zivile Ciuladaite, Vytautas Šliužas, Violeta Mikštienė, Vaidutis Kučinskas

    Published 2016
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  3. 3
    A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report

    A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report by Evelina Siavrienė, Gunda Petraitytė, Violeta Mikštienė, Tautvydas Rančelis, Živilė Maldžienė, Aušra Morkūnienė, Jekaterina Byčkova, Algirdas Utkus, Vaidutis Kučinskas, Eglė Preikšaitienė

    Published 2019
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