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1
Expanding the Phenotype of B3GALNT2-Related Disorders
In: Genes; Volume 13; Issue 4; Pages: 694 (2022)
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2
Main Concept, Sequencing, and Story Grammar Analyses of Cinderella Narratives in a Large Sample of Persons with Aphasia
In: Speech Pathology and Audiology Faculty Research and Publications (2021)
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3
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
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4
The Embodied Modelling of Gestural Sequencing in Speech
Simko, Juraj. - : University College Dublin. School of Computer Science and Informatics, 2021
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5
Productive Failure in Virtual Language Learning for English
Rahayu, Puji. - : The University of Sydney, 2021. : Faculty of Arts and Social Sciences, Sydney School of Education and Social Work, 2021
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6
Criterios de selección y secuenciación textual en la enseñanza de inglés con fines específicos: Aspectos teóricos y principios metodológicos
In: LFE: Revista de lenguas para fines específicos, ISSN 1133-1127, Vol. 27, Nº 1, 2021, pags. 168-184 (2021)
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7
Changes in Activity and Community Composition Shape Bacterial Responses to Size-Fractionated Marine DOM
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8
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://www.hal.inserm.fr/inserm-02964365 ; American Journal of Human Genetics, Elsevier (Cell Press), 2020, 107 (4), pp.727-742. ⟨10.1016/j.ajhg.2020.08.013⟩ (2020)
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9
Transcriptomic Profiling of DAF-7/TGFβ Pathway Mutants in C. elegans
In: Genes ; Volume 11 ; Issue 3 (2020)
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10
Nueva manera de trabajar en la secuencia gramatical para la enseñanza del español como segunda lengua
In: South East Coastal Conference on Languages & Literatures (SECCLL) (2020)
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11
Phonotactic learning with neural language models
In: Proceedings of the Society for Computation in Linguistics (2020)
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12
Les interrogatives partielles dans un corpus de théâtre contemporain
In: Langages, N 217, 1, 2020-03-13, pp.23-38 (2020)
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13
Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family
In: ISSN: 0301-4851 ; EISSN: 1573-4978 ; Molecular Biology Reports ; https://hal-riip.archives-ouvertes.fr/pasteur-03565723 ; Molecular Biology Reports, Springer Verlag, 2019, 46 (4), pp.4185 - 4193. ⟨10.1007/s11033-019-04869-6⟩ (2019)
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14
Chunking of phonological units in speech sequencing
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15
Maximize Resolution or Minimize Error? Using Genotyping-By-Sequencing to Investigate the Recent Diversification of Helianthemum (Cistaceae)
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16
Mitogenomes illuminate the origin and migration patterns of the indigenous people of the Canary Islands.
In: PloS one, vol 14, iss 3 (2019)
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17
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
In: Genetics in medicine : official journal of the American College of Medical Genetics, vol 21, iss 8 (2019)
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18
Likely Pathogenic Variants in One Third of Non-Syndromic Discontinuous Cleft Lip and Palate Patients
In: Genes ; Volume 10 ; Issue 10 (2019)
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19
Nueva manera de trabajar en la secuencia gramatical para la enseñanza del español como segunda lengua
In: South East Coastal Conference on Languages & Literatures (SECCLL) (2019)
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20
Category Positioning - A Qualitative Content Analysis Approach to Explore the Subjective Importance of a Research Topic Using the Example of the Transition From School to University
In: Forum Qualitative Sozialforschung / Forum: Qualitative Social Research ; 20 ; 3 ; Qualitative Content Analysis I (2019)
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