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Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.Journal of Medical Genetics, 2001, 38 (2), pp.121-5. ⟨10.1136/jmg.38.2.121⟩
Journal articles
hal-01158343v1
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Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French casesClinical Genetics, 2018, 94 (1), pp.141-152. ⟨10.1111/cge.13254⟩
Journal articles
hal-02393652v1
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Use of magnetic resonance image registration to estimate displacement in the human earcanal due to the insertion of in-ear devicesJournal of the Acoustical Society of America, 2019, 146 (4), pp.2452-2465. ⟨10.1121/1.5126857⟩
Journal articles
hal-02370631v1
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