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- Publisher Website: 10.1002/ajmg.a.38321
- Scopus: eid_2-s2.0-85026372837
- WOS: WOS:000407839600024
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Article: Agenesis of the corpus callosum, Developmental delay, Autism spectrum disorder, facial dysmorphism, and Posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion
| Title | Agenesis of the corpus callosum, Developmental delay, Autism spectrum disorder, facial dysmorphism, and Posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion |
|---|---|
| Authors | |
| Keywords | agenesis of corpus callosum (ACC) array-CGH autism spectrum disorder chromosome 10p11.22 corneal dystrophy deletion ZEB1 |
| Issue Date | 2017 |
| Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jabout/33129/ProductInformation.html |
| Citation | American Journal of Medical Genetics Part A, 2017, v. 173 n. 9, p. 2467-2471 How to Cite? |
| Persistent Identifier | http://hdl.handle.net/10722/241777 |
| ISSN | 2023 Impact Factor: 1.7 2023 SCImago Journal Rankings: 0.718 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Chaudhry, A | - |
| dc.contributor.author | Chung, BHY | - |
| dc.contributor.author | Stavropoulos, DJ | - |
| dc.contributor.author | Araya, MP | - |
| dc.contributor.author | Ali, A | - |
| dc.contributor.author | Heon, E | - |
| dc.contributor.author | Chitayat, D | - |
| dc.date.accessioned | 2017-06-20T01:48:25Z | - |
| dc.date.available | 2017-06-20T01:48:25Z | - |
| dc.date.issued | 2017 | - |
| dc.identifier.citation | American Journal of Medical Genetics Part A, 2017, v. 173 n. 9, p. 2467-2471 | - |
| dc.identifier.issn | 1552-4825 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/241777 | - |
| dc.language | eng | - |
| dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jabout/33129/ProductInformation.html | - |
| dc.relation.ispartof | American Journal of Medical Genetics Part A | - |
| dc.rights | American Journal of Medical Genetics Part A. Copyright © John Wiley & Sons, Inc. | - |
| dc.rights | Preprint: This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Postprint: This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Special Statement for Preprint only Before publication: 'This is a preprint of an article accepted for publication in [The Journal of Pathology] Copyright © ([year]) ([Pathological Society of Great Britain and Ireland])'. After publication: the preprint notice should be amended to follows: 'This is a preprint of an article published in [include the complete citation information for the final version of the Contribution as published in the print edition of the Journal]' For Cochrane Library/ Cochrane Database of Systematic Reviews, add statement & acknowledgement : ‘This review is published as a Cochrane Review in the Cochrane Database of Systematic Reviews 20XX, Issue X. Cochrane Reviews are regularly updated as new evidence emerges and in response to comments and criticisms, and the Cochrane Database of Systematic Reviews should be consulted for the most recent version of the Review.’ Please include reference to the Review and hyperlink to the original version using the following format e.g. Authors. Title of Review. Cochrane Database of Systematic Reviews 20XX, Issue #. Art. No.: CD00XXXX. DOI: 10.1002/14651858.CD00XXXX (insert persistent link to the article by using the URL: http://dx.doi.org/10.1002/14651858.CD00XXXX) (This statement should refer to the most recent issue of the Cochrane Database of Systematic Reviews in which the Review published.) | - |
| dc.subject | agenesis of corpus callosum (ACC) | - |
| dc.subject | array-CGH | - |
| dc.subject | autism spectrum disorder | - |
| dc.subject | chromosome 10p11.22 | - |
| dc.subject | corneal dystrophy | - |
| dc.subject | deletion | - |
| dc.subject | ZEB1 | - |
| dc.title | Agenesis of the corpus callosum, Developmental delay, Autism spectrum disorder, facial dysmorphism, and Posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion | - |
| dc.type | Article | - |
| dc.identifier.email | Chung, BHY: bhychung@hku.hk | - |
| dc.identifier.authority | Chung, BHY=rp00473 | - |
| dc.identifier.doi | 10.1002/ajmg.a.38321 | - |
| dc.identifier.scopus | eid_2-s2.0-85026372837 | - |
| dc.identifier.hkuros | 272684 | - |
| dc.identifier.volume | 173 | - |
| dc.identifier.issue | 9 | - |
| dc.identifier.spage | 2467 | - |
| dc.identifier.epage | 2471 | - |
| dc.identifier.isi | WOS:000407839600024 | - |
| dc.publisher.place | United States | - |
| dc.identifier.issnl | 1552-4825 | - |