Showing 1 - 4 results of 4 for search 'Sandra Chantot-Bastaraud', query time: 0.03s Refine Results
  1. 1
    When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20

    When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20 by Marguerite Hureaux, Sandra Chantot-Bastaraud, Kévin Cassinari, Edouard Martinez Casado, Ariane Cuny, Thierry Frébourg, Rosa Vargas-Poussou, Anne-Claire Bréhin

    Published 2021-05-01
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  2. 2
    Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction

    Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction by Sandra Chantot-Bastaraud, Svea Stratmann, Frédéric Brioude, Matthias Begemann, Miriam Elbracht, Luitgard Graul-Neumann, Madeleine Harbison, Irène Netchine, Thomas Eggermann

    Published 2017-07-01
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  3. 3
    Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness

    Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness by Cora Cravero, Vincent Guinchat, Jean Xavier, Camille Meunier, Lautaro Diaz, Cyril Mignot, Diane Doummar, Sandra Chantot-Bastaraud, Angèle Consoli, David Cohen

    Published 2017-01-01
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  4. 4
    Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts.

    Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts. by Celia Ravel, Sandra Chantot-Bastaraud, Clementine Chalmey, Luis Barreiro, Isabelle Aknin-Seifer, Jerome Pfeffer, Isabelle Berthaut, E Emmanuelle Mathieu, Jacqueline Mandelbaum, Jean-Pierre Siffroi, Ken McElreavey, Anu Bashamboo

    Published 2009-01-01
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