F. Boidein

Most-cited papers

1. A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay.

   S. Bouquillon, J. Andrieux, E. Landais, B. Duban‐Bedu +6 more

   2011European Journal of Medical Genetics28 citations

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2. Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite

   A. Dharmadhikari, T. Gambin, P. Szafranski, Wen-Jian Cao +15 more

   2014BMC Medical Genetics13 citations Open access

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3. [Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].

   F. Cneude, S. Sukno, F. Boidein, M. Dehouck +2 more

   1999Revue neurologique (Paris)5 citations

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4. [Prescribing ritalin in combined modality management of hyperactivity with attention deficit].

   C. Bricard, F. Boidein

   2001L'Encephale2 citations

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5. [Benign infantile convulsions. French collaborative study].

   A. Gautier, F. Pouplard, N. Bednarek, J. Motte +7 more

   1999Archives de pédiatrie2 citations

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6. Case Report of a Patient With Speech Delay and Behavioral Disorders Associated with Neuroblastoma. Possible Role of SMARCA4

   A. Defachelles, Nathalie Clément, B. Duban‐Bedu, F. Boidein +6 more

   20140 citations

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7. Un diagnostic cytogénétique difficile de monosomie 4p

   G. Vittu, M. Croquette, F. Boidein, J. Cousin

   19880 citations

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8. [A difficult cytogenetic diagnosis of 4p monosomy].

   G. Vittu, M. Croquette, F. Boidein, J. Cousin

   1988Journal de genetique humaine0 citations

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