Search Results - "Du Boullay, Hélène"

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    Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome by LEROY, Chrystel, FOUVEAUT, Corinne, LECLERCQ, Sandrine, JACQUEMONT, Sébastien, DU BOULLAY, Hélène, LESPINASSE, James, DELPECH, Marc, DUPONT, Jean-Michel, HARDELIN, Jean-Pierre, DODE, Catherine

    Published in European journal of human genetics : EJHG (01-07-2008)
    “…Kallmann syndrome is a developmental disease that combines hypogonadotropic hypogonadism and anosmia. Putative loss-of-function mutations in PROKR2 or PROK2,…”
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    Journal Article
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