• Refine your search:
  • 
    Keyword:
    
    • Social support (2)
    • [SDV.GEN]Life Sciences [q-bio] / Genetics (2)
    • 7q11 (1)
    • 7q11.23 (1)
    • Autism (1)
    • Autistic disorder (1)
    • Behavior (1)
    • Behavioral disorders (1)
    • Diagnostic medicine (1)
    • Down syndrome (1)
    •   more
  • 
    Creator / Publisher
  • 
    Year
  • 
    Medium
  • 
    Type
  • 
    BLLDB-Access

Search in the Catalogues and Directories

All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 6 of 6 1 Care management in a French cohort with down syndrome from the AnDDI-Rares/CNSA study Roux-Levy, Pierre-Henri; Sanlaville, Damien; DE FREMINVILLE, Benedicte... In: ISSN: 1769-7212 ; European Journal of Medical Genetics ; https://hal.archives-ouvertes.fr/hal-03403503 ; European Journal of Medical Genetics, Elsevier, 2021, 64 (10), ⟨10.1016/j.ejmg.2021.104290⟩ (2021) BASE Show details 2 Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome Roux-Levy, Pierre-Henri; Bournez, Marie; Masurel, Alice... In: ISSN: 1769-7212 ; European Journal of Medical Genetics ; https://hal.umontpellier.fr/hal-03338019 ; European Journal of Medical Genetics, Elsevier, 2020, 63 (12), pp.104064. ⟨10.1016/j.ejmg.2020.104064⟩ (2020) BASE Show details 3 Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome. Tordjman, Sylvie; Anderson, George; Cohen, David... In: ISSN: 2040-2392 ; Molecular Autism ; https://www.hal.inserm.fr/inserm-00868741 ; Molecular Autism, BioMed Central, 2013, 4 (1), pp.29. ⟨10.1186/2040-2392-4-29⟩ (2013) BASE Show details 4 Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype Tordjman, Sylvie; Anderson, George M.; Botbol, Michel... In: ISSN: 1932-6203 ; EISSN: 1932-6203 ; PLoS ONE ; https://hal.archives-ouvertes.fr/hal-01439710 ; PLoS ONE, Public Library of Science, 2012, 7 (3), ⟨10.1371/journal.pone.0030778⟩ (2012) BASE Show details 5 Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. Passemard, Sandrine; Titomanlio, Luigi; Elmaleh, Monique... In: ISSN: 0028-3878 ; EISSN: 1526-632X ; Neurology ; https://www.hal.inserm.fr/inserm-00420406 ; Neurology, American Academy of Neurology, 2009, 73 (12), pp.962-9. ⟨10.1212/WNL.0b013e3181b8799a⟩ (2009) BASE Show details 6 Autism, language delay and mental retardation in a patient with 7q11 duplication. ; : Autism and 7q11 duplication Depienne, Christel; Héron, Delphine; Betancur, Catalina... In: ISSN: 0022-2593 ; EISSN: 1468-6244 ; Journal of Medical Genetics ; https://www.hal.inserm.fr/inserm-00166907 ; Journal of Medical Genetics, BMJ Publishing Group, 2007, 44 (7), pp.452-8. ⟨10.1136/jmg.2006.047092⟩ (2007) BASE Show details

Mobile view All Catalogues UB Frankfurt Linguistik 0 IDS Mannheim 0 OLC Linguistik 0 UB Frankfurt Retrokatalog 0 DNB Subject Category Language 0 Institut für Empirische Sprachwissenschaft 0 Leibniz-Centre General Linguistics (ZAS) 0 Bibliographies BLLDB 0 BDSL 0 IDS Bibliografie zur deutschen Grammatik 0 IDS Bibliografie zur Gesprächsforschung 0 IDS Konnektoren im Deutschen 0 IDS Präpositionen im Deutschen 0 IDS OBELEX meta 0 MPI-SHH Linguistics Collection 0 MPI for Psycholinguistics 0 Linked Open Data catalogues Annohub 0 Online resources Link directory 0 Journal directory 0 Database directory 0 Dictionary directory 0 Open access documents BASE 6 Linguistik-Repository 0 IDS Publikationsserver 0 Online dissertations 0 Language Description Heritage 0