Search Results - Roulez, Françoise

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  1. 1
    Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes

    Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes by Lang, Elena, Koller, Samuel, Bähr, Luzy, Töteberg-Harms, Marc, Atac, David, Roulez, Françoise, Bahr, Angela, Steindl, Katharina, Feil, Silke, Berger, Wolfgang, Gerth-Kahlert, Christina

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  2. 2
    Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations

    Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations by D'haene, Barbara, Meire, Françoise, Claerhout, Ilse, Kroes, Hester Y, Plomp, Astrid, Arens, Yvonne H, de Ravel, Thomy, Casteels, Ingele, De Jaegere, Sarah, Hooghe, Sally, Wuyts, Wim, van den Ende, Jenneke, Roulez, Françoise, Veenstra-Knol, Hermine E, Oldenburg, Rogier A, Giltay, Jacques, Verheij, Johanna B G M, de Faber, Jan-Tjeerd, Menten, Björn, De Paepe, Anne, Kestelyn, Philippe, Leroy, Bart P, De Baere, Elfride

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  3. 3
    Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes

    Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes by Meire, Françoise, Delpierre, Isabelle, Brachet, Cecile, Roulez, Françoise, Van Nechel, Christian, Depasse, Fanny, Christophe, Catherine, Menten, Björn, De Baere, Elfride

    Published in Molecular vision
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  4. 4
    LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma

    LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma by Désir, Julie, Sznajer, Yves, Depasse, Fanny, Roulez, Françoise, Schrooyen, Marc, Meire, Françoise, Abramowicz, Marc

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  5. 5
    Papillorenal syndrome with secondary serous retinal detachment: family history can help the diagnosis

    Papillorenal syndrome with secondary serous retinal detachment: family history can help the diagnosis by Roulez, Francoise

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  6. 6
    Corneal Opacities in the Hallermann-Streiff Syndrome

    Corneal Opacities in the Hallermann-Streiff Syndrome by Roulez, Françoise M., Schuil, Josée, Meire, Françoise M.

    Published in Ophthalmic genetics
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