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SAE technical paper series, Volume 710027.
The paper discusses the SAE Technical Program on RFI Measurements and is basically a tutorial review of radio frequency interference/electromagnetic... 
Electronic equipment | Radio equipment | Noise
eJournal
2008, 1st ed., ISBN 0080447015, xix, 313
Researchers and clinicians working with Obsessive-Compulsive Disorders (OCD) and related disorders who need the most current information available will find... 
Psychology | Obsessive-compulsive disorder
Book
Current Psychiatry Reviews, ISSN 1573-4005, 01/2014, Volume 10, Issue 4, pp. 284 - 288
Journal Article
Journal Article
2012, ESL & applied linguistics professional series, ISBN 0415891671, ix, 362
"What general principles should inform a socioculturally sensitive pedagogy for teaching English as an International Language and what practices would be... 
Study and teaching | English language | Foreign speakers | Lingua francas | Language & Linguistics | Bilingualism / ESL | World Englishes | Applied Linguistics | FOREIGN LANGUAGE STUDY / English as a Second Language
Book
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/1994, Volume 91, Issue 24, pp. 11762 - 11766
... administration of phosphorothioate antisense oligodeoxynucleotides NICHOLAS M. DEAN* AND ROBERT MCKAY Department of Molecular Pharmacology, ISIS Pharmaceuticals, Carlsbad... 
Messenger RNA | 3T3 cells | RNA | NIH 3T3 cells | Liver | Oligonucleotides | Cell lines | Cultured cells | Mice | Endothelial cells | CELLS | PHARMACOKINETICS | STABILITY | MULTIDISCIPLINARY SCIENCES | DOWN-REGULATION | BIODISTRIBUTION | HYBRIDIZATION | CDNA | NF-KAPPA-B | OLIGONUCLEOTIDES | Oligodeoxynucleotides | Protein kinases | Research
Journal Article
Diabetes, ISSN 0012-1797, 04/2002, Volume 51, Issue 4, pp. 1028 - 1034
Journal Article
by Fitzgerald, T.W and Gerety, S.S and Jones, W.D and Van Kogelenberg, M and King, D.A and McRae, J and Morley, K.I and Parthiban, V and Al-Turki, S and Ambridge, K and Barrett, D.M and Bayzetinova, T and Clayton, S and Coomber, E.L and Gribble, S and Jones, P and Krishnappa, N and Mason, L.E and Middleton, A and Miller, R and Prigmore, E and Rajan, D and Sifrim, A and Tivey, A.R and Ahmed, M and Akawi, N and Andrews, R and Anjum, U and Archer, H and Armstrong, R and Balasubramanian, M and Banerjee, R and Baralle, D and Batstone, P and Baty, D and Bennett, C and Berg, J and Bernhard, B and Bevan, A.P and Blair, E and Blyth, M and Bohanna, D and Bourdon, L and Bourn, D and Brady, A and Bragin, E and Brewer, C and Brueton, L and Brunstrom, K and Bumpstead, S.J and Bunyan, D.J and Burn, J and Burton, J and Canham, N and Castle, B and Chandler, K and Clasper, S and Clayton-Smith, J and Cole, T and Collins, A and Collinson, M.N and Connell, F and Cooper, N and Cox, H and Cresswell, L and Cross, G and Crow, Y and D'Alessandro, M and Dabir, T and Davidson, R and Davies, S and Dean, J and Deshpande, C and Devlin, G and Dixit, A and Dominiczak, A and Donnelly, C and Donnelly, D and Douglas, A and Duncan, A and Eason, J and Edkins, S and Ellard, S and Ellis, P and Elmslie, F and Evans, K and Everest, S and Fendick, T and Fisher, R and Flinter, F and Foulds, N and Fryer, A and Fu, B and Gardiner, C and Gaunt, L and Ghali, N and Gibbons, R and Gomes Pereira, S.L and Goodship, J and Goudie, D and ... and Deciphering Dev Disorders Study and Deciphering Developmental Disorders Study and The Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 03/2015, Volume 519, Issue 7542, pp. 223 - 228
Despite three decades of successful, predominantly phenotype-driven discovery of the genetic causes of monogenic disorders(1), up to half of children with... 
INTELLECTUAL DISABILITY | HUMAN-DISEASE | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | MODEL | AUTISM SPECTRUM DISORDERS | COPY-NUMBER VARIATION | CHILDREN | Rare Diseases - genetics | Humans | Repressor Proteins | Parents | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Dynamin I - genetics | Mutation, Missense - genetics | Polycomb Repressive Complex 1 - genetics | Gene Expression Regulation, Developmental | Transposases - genetics | Female | Nuclear Proteins - genetics | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Guanine Nucleotide Exchange Factors - genetics | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | United Kingdom | Phosphoproteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Zebrafish - genetics | Chromosomal Proteins, Non-Histone - genetics | Carrier Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Animals | Adolescent | Chromosome Aberrations | Genes, Dominant - genetics | Usage | Genomics | Child development deviations | Genetic aspects | Research | Risk factors | Developmental disabilities | Studies | Hypotheses | Genes | Developmental psychology | Families & family life | Genomes | Mutation | Children & youth
Journal Article
Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 06/2012, Volume 4, Issue 6, pp. 515 - 527
Journal Article