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Additional file 1 of When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20

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posted on 2021-05-06, 03:39 authored by Marguerite Hureaux, Sandra Chantot-Bastaraud, Kévin Cassinari, Edouard Martinez Casado, Ariane Cuny, Thierry Frébourg, Rosa Vargas-Poussou, Anne-Claire Bréhin
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    Molecular Cytogenetics

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    Keywords

    Uniparental disomy of chromosome 20Infantile hypercalcemiaCYP24A1Silver-Russell-like syndrome

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    CC BY + CC0

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