Search Results - "Reader RH"

Advances in the Production and Batch Reformatting of Phage Antibody Libraries.

Authors: Reader RH Workman RG Maddison BC et al.

Source: Molecular biotechnology [Mol Biotechnol] 2019 Nov; Vol. 61 (11), pp. 801-815.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer Country of Publication: Switzerland NLM ID: 9423533 Publication Model: Print Cited Medium: Internet ISSN: 1559-0305 (Electronic) Linking ISSN: 10736085 NLM ISO Abbreviation: Mol Biotechnol Subsets: MEDLINE

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.

Authors: Simpson NH Ceroni F Reader RH et al.

Corporate Authors: Simpson NH Ceroni F Reader RH et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Oct; Vol. 23 (10), pp. 1370-7. Date of Electronic Publication: 2015 Jan 14.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.

Authors: Villanueva P Nudel R Hoischen A et al.

Corporate Authors: Villanueva P Nudel R Hoischen A et al.

Source: PLoS genetics [PLoS Genet] 2015 Jun 26; Vol. 11 (6), pp. e1005336. Date of Electronic Publication: 2015 Jun 26 (Print Publication: 2015).

Publication Type: Published Erratum

Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: PubMed not MEDLINE

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Authors: Villanueva P Nudel R Hoischen A et al.

Corporate Authors: Villanueva P Nudel R Hoischen A et al.

Source: PLoS genetics [PLoS Genet] 2015 Mar 17; Vol. 11 (3), pp. e1004925. Date of Electronic Publication: 2015 Mar 17 (Print Publication: 2015).

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Authors: Chen XS Reader RH Hoischen A et al.

Source: Scientific reports [Sci Rep] 2017 Apr 25; Vol. 7, pp. 46105. Date of Electronic Publication: 2017 Apr 25.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

Genome-Wide Studies of Specific Language Impairment.

Authors: Reader RH Covill LE Nudel R et al.

Source: Current behavioral neuroscience reports [Curr Behav Neurosci Rep] 2014; Vol. 1 (4), pp. 242-250.

Publication Type: Review; Journal Article

Journal Info: Publisher: Springer International Publishing AG Country of Publication: Switzerland NLM ID: 101626570 Publication Model: Print Cited Medium: Print ISSN: 2196-2979 (Print) NLM ISO Abbreviation: Curr Behav Neurosci Rep Subsets: PubMed not MEDLINE