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1
Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features
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)
BASE
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2
Heterozygous deletion of the LRFN2 gene is associated with working memory deficits
In: ISSN: 1018-4813 ; EISSN: 1476-5438 ; European Journal of Human Genetics ; https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01405814 ; European Journal of Human Genetics, Nature Publishing Group, 2016, 24 (6), pp.911 - 918. ⟨10.1038/ejhg.2015.221⟩ ; http://www.nature.com/ejhg/journal/v24/n6/full/ejhg2015221a.html (2016)
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3
Class as a semiotic resource in consumer advertising: Markedness, heteroglossia, and commodity temporalities
In: Discourse & society. - London [u.a.] : Sage 25 (2014) 5, 581-599
OLC Linguistik
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4
12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech
Thevenon, Julien; Callier, Patrick; Andrieux, Joris. - : Nature Publishing Group, 2013
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5
Style-shifting in public : new perspectives on stylistic variation
Gibson, Andy; Zhang, Qing; Podesva, Robert J.. - Amsterdam [u.a.] : Benjamins, 2012
BLLDB
UB Frankfurt Linguistik
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6
Social Meaning in Prosodic Variability
In: University of Pennsylvania Working Papers in Linguistics (2011)
BASE
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7
Review
In: Language in society. - London [u.a.] : Cambridge Univ. Press 38 (2009) 1, 138
OLC Linguistik
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