miR-126 Is Involved in Vascular Remodeling under Laminar Shear Stress by Metzinger-Le Meuth, Valérie, Hlawaty, Hanna, Charnaux, Nathalie, Taïbi, Fatiha, M’baya-Moutoula, Eléonore, Haddad, Oualid, Metzinger, Laurent, Mondadori dos Santos, Ana, Massy, Ziad A.

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Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome by Silveira, Henrique Garcia, Steiner, Carlos Eduardo, Toccoli, Giovana, Angeloni, Luise Longo, Heleno, Júlia Lôndero, Spineli-Silva, Samira, Dos Santos, Ana Mondadori, Vieira, Társis Paiva, Melaragno, Maria Isabel, Gil-da-Silva-Lopes, Vera Lúcia

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Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review by Correia-Costa, Gabriela Roldão, Dos Santos, Ana Mondadori, de Leeuw, Nicole, Rigatto, Sumara Zuanazi Pinto, Belangero, Vera Maria Santoro, Steiner, Carlos Eduardo, Gil-da-Silva-Lopes, Vera Lúcia, Vieira, Társis Paiva

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Novel variants in the SOX11 gene: clinical description of seven new patients by Schincariol-Manhe, Beatriz, Campagnolo, Érica, Spineli-Silva, Samira, de Leeuw, Nicole, Correia-Costa, Gabriela Roldão, Pessoa, André, de Souza, Carolina Fischinger Moura, Stevens, Cathy, Javaher, Poupak, Scallet, Helena Fabbri, Mohr, Julia, Biskup, Saskia, Herkert, Johanna C., Pfundt, Rolph, Mehta, Lakshmi, Rekab, Aisha, Elloumi, Houda Zghal, Sanyoura, May, Maciel-Guerra, Andréa Trevas, Gil-da-Silva-Lopes, Vera Lúcia, dos Santos, Ana Mondadori, Vieira, Társis Paiva

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Variants in IKMT2A/I in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome by Silveira, Henrique Garcia, Steiner, Carlos Eduardo, Toccoli, Giovana, Angeloni, Luise Longo, Heleno, Júlia Lôndero, Spineli-Silva, Samira, dos Santos, Ana Mondadori, Vieira, Társis Paiva, Melaragno, Maria Isabel, Gil-da-Silva-Lopes, Vera Lúcia

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