Search Results - "Boidein, Françoise"

Predictive factors of reading in children with developmental language disorder by Macchi, Lucie, Schelstraete, Marie-Anne, Ané, Cécile, Boidein, Françoise, Riquet, Audrey, Casalis, Séverine

“…•Oral language skills are strong predictors of reading skills.•Children with Developmental Language Disorder encounter reading difficulties in higher…”
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A 5.3 Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay by Bouquillon, Sonia, Andrieux, Joris, Landais, Emilie, Duban-Bedu, Bénédicte, Boidein, Françoise, Lenne, Bruno, Vallée, Louis, Leal, Teresinha, Doco-Fenzy, Martine, Delobel, Bruno

“…Abstract Interstitial 18q deletions encompassing band 18q12.3 define the del(18)(q12.2q21.1) syndrome. Usual manifestations are mild dysmorphic features,…”
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A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay by Bouquillon, Sonia, Andrieux, Joris, Landais, Emilie, Duban-Bedu, Bénédicte, Boidein, Françoise, Lenne, Bruno, Vallée, Louis, Leal, Teresinha, Doco-Fenzy, Martine, Delobel, Bruno

“…Interstitial 18q deletions encompassing band 18q12.3 define the del(18)(q12.2q21.1) syndrome. Usual manifestations are mild dysmorphic features, mental…”
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Case Report of a Patient With Speech Delay and Behavioral Disorders Associated with Neuroblastoma. Possible Role of SMARCA4 by Defachelles, Anne-Sophie, Clément, Nathalie, Duban-Bedu, Bénédicte, Boidein, Françoise, Pierron, Gaëlle, Ferrand, Sandrine, Peuchmaur, Michel, Delattre, Olivier, Bourdeaut, Franck, Schleiermacher, Gudrun

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Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite by Dharmadhikari, Avinash V, Gambin, Tomasz, Szafranski, Przemyslaw, Cao, Wenjian, Probst, Frank J, Jin, Weihong, Fang, Ping, Gogolewski, Krzysztof, Gambin, Anna, George-Abraham, Jaya K, Golla, Sailaja, Boidein, Francoise, Duban-Bedu, Benedicte, Delobel, Bruno, Andrieux, Joris, Becker, Kerstin, Holinski-Feder, Elke, Cheung, Sau Wai, Stankiewicz, Pawel

“…Point mutations or genomic deletions of FOXF1 result in a lethal developmental lung disease Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins…”
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