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Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features
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In: ISSN: 0022-2593 ; EISSN: 1468-6244 ; Journal of Medical Genetics ; https://hal-univ-bourgogne.archives-ouvertes.fr/hal-02064139 ; Journal of Medical Genetics, BMJ Publishing Group, 2018, 55 (6), pp.jmedgenet-2017-104956. ⟨10.1136/jmedgenet-2017-104956⟩ ; https://jmg.bmj.com/content/55/6/359.long (2018)
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Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature
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In: ISSN: 1471-2350 ; BMC Medical Genetics ; https://www.hal.inserm.fr/inserm-02305085 ; BMC Medical Genetics, BioMed Central, 2017, 18 (1), pp.9. ⟨10.1186/s12881-017-0371-1⟩ (2017)
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