Search Results - Brφndum-Nielsen, K

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    Clinical features and molecular genetic analysis of a boy with Prader‐Willi syndrome caused by an imprinting defect

    Clinical features and molecular genetic analysis of a boy with Prader‐Willi syndrome caused by an imprinting defect by Schulze, A, Hansen, C, Bækgaard, P, Blichfeldt, S, Petersen, MB, Tommerup, N, Brφndum‐Nielsen, K

    Published in Acta Paediatrica
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    Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect

    Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect by Schulze, A, Hansen, C, Bækgaard, P, Blichfeldt, S, Petersen, MB, Tommerup, N, Brφndum-Nielsen, K

    Published in Acta Pædiatrica
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