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Phase 2 of CATALISE: a multinational and multidisciplinary Delphi consensus study of problems with language development: terminology
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Phase 2 of CATALISE: a multinational and multidisciplinary Delphi consensus study of problems with language development: Terminology
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Phase 2 of CATALISE: a multinational and multidisciplinary Delphi consensus study of problems with language development: Terminology
Bishop, Dorothy V.M.; Snowling, Margaret J.; Thompson, Paul A.. - : John Wiley and Sons Inc., 2017
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4
CATALISE: a multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children
Norbury, Courtenay; Leonard, Laurence; McCartney, Elspeth. - : Public Library Science, 2016
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CATALISE : a multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children
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CATALISE: A multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children
In: Communication Sciences and Disorders Publications (2016)
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7
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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8
Associations of HLA alleles with specific language impairment
Nudel, Ron; Simpson, Nuala H; Baird, Gillian. - : BioMed Central, 2014
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9
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
Fisher, Simon E.; Newbury, Dianne F.; Simpson, Nuala H.. - : Nature Publishing Group, 2014
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10
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
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11
Associations of HLA alleles with specific language impairment
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12
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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13
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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14
Interpretation of compound nouns by adolescents with specific language impairment and autism spectrum disorders: an investigation of phenotypic overlap
In: International journal of speech language pathology. - Abingdon : Informa Healthcare 14 (2012) 4, 307-317
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15
Individual common variants exert weak effects on the risk for autism spectrum disorders.
In: Human molecular genetics, vol 21, iss 21 (2012)
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16
Individual common variants exert weak effects on the risk for autism spectrum disorders.
In: ISSN: 0964-6906 ; EISSN: 1460-2083 ; Human Molecular Genetics ; https://www.hal.inserm.fr/inserm-00723650 ; Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (21), pp.4781-92. ⟨10.1093/hmg/dds301⟩ (2012)
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17
Individual common variants exert weak effects on the risk for autism spectrum disorders ...
Folstein, Susan E.; Crawford, Emily L.; Glessner, Joseph T.. - : The University of North Carolina at Chapel Hill University Libraries, 2012
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18
Individual common variants exert weak effects on the risk for autism spectrum disorders
Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012
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19
Individual common variants exert weak effects on risk for Autism Spectrum Disorders
Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012
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20
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012
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