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Article: 22q11.2 deletion syndrome in diverse populations

Title22q11.2 deletion syndrome in diverse populations
Authors
Kruszka, PAddissie, YAMcGinn, DEPorras, ARBiggs, EShare, MCrowley, TBChung, BHYMok, TKGMAK, CCYMuthukumarasamy, PThong, MKSiriseria, NDDissanayake, VHWPaththinige, CSPrabodha, LBLMishra, RShotelersuk, VEkure, ENSokunbi, OJKalu, NFerreira, CRDuncan, JMPatil, SJJones, KLKaplan, JDAbdul-Rahman, OAUwineza, AMutesa, LMoresco, AObregon, MGRichieri-Costa, AGil-da-Silva-Lopes, VLAdeyemo, AASummar, MZackai, EHMcDonald-McGinn, DMLinguraru, MGMuenke, M
Keywords22q11.2 Deletion syndrome
DiGeorge syndrome
diverse populations
facial analysis technology
Velocardiofacial Syndrome
Issue Date2017
PublisherJohn 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, p. 879-888 How to Cite?
DOI: http://dx.doi.org/10.1002/ajmg.a.38199
Persistent Identifierhttp://hdl.handle.net/10722/241616
ISSN
1552-4825
2021 Impact Factor: 2.578
2020 SCImago Journal Rankings: 1.064
PubMed Central ID
PMC5363275
ISI Accession Number ID
WOS:000397855700006

 

DC FieldValueLanguage
dc.contributor.authorKruszka, P-
dc.contributor.authorAddissie, YA-
dc.contributor.authorMcGinn, DE-
dc.contributor.authorPorras, AR-
dc.contributor.authorBiggs, E-
dc.contributor.authorShare, M-
dc.contributor.authorCrowley, TB-
dc.contributor.authorChung, BHY-
dc.contributor.authorMok, TKG-
dc.contributor.authorMAK, CCY-
dc.contributor.authorMuthukumarasamy, P-
dc.contributor.authorThong, MK-
dc.contributor.authorSiriseria, ND-
dc.contributor.authorDissanayake, VHW-
dc.contributor.authorPaththinige, CS-
dc.contributor.authorPrabodha, LBL-
dc.contributor.authorMishra, R-
dc.contributor.authorShotelersuk, V-
dc.contributor.authorEkure, EN-
dc.contributor.authorSokunbi, OJ-
dc.contributor.authorKalu, N-
dc.contributor.authorFerreira, CR-
dc.contributor.authorDuncan, JM-
dc.contributor.authorPatil, SJ-
dc.contributor.authorJones, KL-
dc.contributor.authorKaplan, JD-
dc.contributor.authorAbdul-Rahman, OA-
dc.contributor.authorUwineza, A-
dc.contributor.authorMutesa, L-
dc.contributor.authorMoresco, A-
dc.contributor.authorObregon, MG-
dc.contributor.authorRichieri-Costa, A-
dc.contributor.authorGil-da-Silva-Lopes, VL-
dc.contributor.authorAdeyemo, AA-
dc.contributor.authorSummar, M-
dc.contributor.authorZackai, EH-
dc.contributor.authorMcDonald-McGinn, DM-
dc.contributor.authorLinguraru, MG-
dc.contributor.authorMuenke, M-
dc.date.accessioned2017-06-20T01:46:08Z-
dc.date.available2017-06-20T01:46:08Z-
dc.date.issued2017-
dc.identifier.citationAmerican Journal of Medical Genetics Part A, 2017, v. 173, p. 879-888-
dc.identifier.issn1552-4825-
dc.identifier.urihttp://hdl.handle.net/10722/241616-
dc.languageeng-
dc.publisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jabout/33129/ProductInformation.html-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.rightsAmerican Journal of Medical Genetics Part A. Copyright © John Wiley & Sons, Inc.-
dc.rightsPreprint: 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.subject22q11.2 Deletion syndrome-
dc.subjectDiGeorge syndrome-
dc.subjectdiverse populations-
dc.subjectfacial analysis technology-
dc.subjectVelocardiofacial Syndrome-
dc.title22q11.2 deletion syndrome in diverse populations-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.emailMok, TKG: gtkmok@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.doi10.1002/ajmg.a.38199-
dc.identifier.pmcidPMC5363275-
dc.identifier.scopuseid_2-s2.0-85015933718-
dc.identifier.hkuros272701-
dc.identifier.volume173-
dc.identifier.spage879-
dc.identifier.epage888-
dc.identifier.isiWOS:000397855700006-
dc.publisher.placeUnited States-
dc.identifier.issnl1552-4825-

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