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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Congenital distichiasisBMJ (Online), 2019-06, Vol.365, p.l2234 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go tohttp://group.bmj.com/group/rights-licensing/permissions2019BMJ ;ISSN: 0959-8138 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.l2234Full text available |
| 2 |
Material Type: Article
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Anti-epileptic drugs in fathers . . . and other storiesBMJ (Online), 2020-09, Vol.370, p.m3514 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go tohttp://group.bmj.com/group/rights-licensing/permissions2020BMJ ;ISSN: 1756-1833 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.m3514Full text available |
| 3 |
Material Type: Article
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Gene therapy comes of ageScience (American Association for the Advancement of Science), 2018-01, Vol.359 (6372) [Peer Reviewed Journal]Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. ;Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.aan4672 ;PMID: 29326244Digital Resources/Online E-Resources |
| 4 |
Material Type: Article
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Genetics and Genomics of Congenital Heart DiseaseCirculation research, 2017-03, Vol.120 (6), p.923-940 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Mar 17, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/circresaha.116.309140 ;PMID: 28302740Full text available |
| 5 |
Material Type: Article
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Molecular findings from 537 individuals with inherited retinal diseaseJournal of medical genetics, 2016-11, Vol.53 (11), p.761-767 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/. ;Copyright: 2016 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2016 ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2016-103837 ;PMID: 27208204 ;CODEN: JMDGAEFull text available |
| 6 |
Material Type: Article
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De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesScience (American Association for the Advancement of Science), 2015-12, Vol.350 (6265), p.1262-1266 [Peer Reviewed Journal]Copyright © 2015 American Association for the Advancement of Science ;Copyright © 2015, American Association for the Advancement of Science. ;Copyright © 2015, American Association for the Advancement of Science ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.aac9396 ;PMID: 26785492 ;CODEN: SCIEASDigital Resources/Online E-Resources |
| 7 |
Material Type: Article
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The hidden pupil: a unilateral congenital corectopiaBMJ (Online), 2020-03, Vol.368, p.m847 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go tohttp://group.bmj.com/group/rights-licensing/permissions2020BMJ ;ISSN: 1756-1833 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.m847Full text available |
| 8 |
Material Type: Article
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P79 Children with complex congenital heart disease: who needs a pre-flight hypoxic challenge test?Thorax, 2017-12, Vol.72 (Suppl 3), p.A126 [Peer Reviewed Journal]2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2017 © 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0040-6376 ;EISSN: 1468-3296 ;DOI: 10.1136/thoraxjnl-2017-210983.221Full text available |
| 9 |
Material Type: Article
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Acetmainophen Effect on Prostaglandin E2; A Mechanism for Patent Ductus Arteriosus ClosurePediatrics (Evanston), 2017-09, Vol.140 (1_MeetingAbstract), p.52-52 [Peer Reviewed Journal]Copyright American Academy of Pediatrics Sep 2017 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.140.1MA.52Digital Resources/Online E-Resources |
| 10 |
Material Type: Article
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Updated Strategies for Pulse Oximetry Screening for Critical Congenital Heart DiseasePediatrics (Evanston), 2020-07, Vol.146 (1), p.1 [Peer Reviewed Journal]Copyright American Academy of Pediatrics Jul 2020 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2019-1650Digital Resources/Online E-Resources |
| 11 |
Material Type: Article
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The EULAR points to consider for use of antirheumatic drugs before pregnancy, and during pregnancy and lactationAnnals of the rheumatic diseases, 2016-05, Vol.75 (5), p.795-810 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Copyright: 2016 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;ISSN: 0003-4967 ;EISSN: 1468-2060 ;DOI: 10.1136/annrheumdis-2015-208840 ;PMID: 26888948 ;CODEN: ARDIAOFull text available |
| 12 |
Material Type: Article
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Patent Ductus Arteriosus of the Preterm InfantPediatrics (Evanston), 2020-11, Vol.146 (5), p.e20201209 [Peer Reviewed Journal]Copyright © 2020 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Nov 1, 2020 ;Copyright © 2020 by the American Academy of Pediatrics 2020 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2020-1209 ;PMID: 33093140Digital Resources/Online E-Resources |
| 13 |
Material Type: Article
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Hearing loss and congenital CMV infection: a systematic reviewPediatrics (Evanston), 2014-11, Vol.134 (5), p.972-982 [Peer Reviewed Journal]Copyright © 2014 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Nov 2014 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2014-1173 ;PMID: 25349318 ;CODEN: PEDIAUFull text available |
| 14 |
Material Type: Article
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Molecular Pathophysiology of Congenital Long QT SyndromePhysiological reviews, 2017-01, Vol.97 (1), p.89-134 [Peer Reviewed Journal]Copyright © 2017 the American Physiological Society. ;Copyright American Physiological Society Jan 2017 ;Copyright © 2017 the American Physiological Society 2017 American Physiological Society ;ISSN: 0031-9333 ;EISSN: 1522-1210 ;DOI: 10.1152/physrev.00008.2016 ;PMID: 27807201 ;CODEN: PHREA7Full text available |
| 15 |
Material Type: Article
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Patent Ductus Arteriosus in Preterm InfantsPediatrics (Evanston), 2016-01, Vol.137 (1), p.1 [Peer Reviewed Journal]Copyright © 2016 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Jan 2016 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2015-3730 ;PMID: 26672023 ;CODEN: PEDIAUFull text available |
| 16 |
Material Type: Article
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DIAGNOSIS OF ENDOCRINE DISEASE: Congenital hypothyroidism: update and perspectivesEuropean journal of endocrinology, 2018-12, Vol.179 (6), p.R297-R317 [Peer Reviewed Journal]2018 European Society of Endocrinology ;Copyright BioScientifica Ltd. Dec 2018 ;ISSN: 0804-4643 ;EISSN: 1479-683X ;DOI: 10.1530/EJE-18-0383 ;PMID: 30324792Full text available |
| 17 |
Material Type: Article
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Probable congenital SARS-CoV-2 infection in a neonate born to a woman with active SARS-CoV-2 infectionCanadian Medical Association journal (CMAJ), 2020-06, Vol.192 (24), p.E647-E650 [Peer Reviewed Journal]COPYRIGHT 2020 Joule Inc. ;Copyright Joule Inc Jun 15, 2020 ;2020 Joule Inc. or its licensors 2020 ;ISSN: 0820-3946 ;EISSN: 1488-2329 ;DOI: 10.1503/cmaj.200821 ;PMID: 32409520Full text available |
| 18 |
Material Type: Article
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Rapid development of a DNA vaccine for Zika virusScience (American Association for the Advancement of Science), 2016-10, Vol.354 (6309), p.237-240 [Peer Reviewed Journal]Copyright © 2016 American Association for the Advancement of Science ;Copyright © 2016, American Association for the Advancement of Science. ;Copyright © 2016, American Association for the Advancement of Science ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.aai9137 ;PMID: 27708058 ;CODEN: SCIEASDigital Resources/Online E-Resources |
| 19 |
Material Type: Article
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Changing Landscape of Congenital Heart DiseaseCirculation research, 2017-03, Vol.120 (6), p.908-922 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Mar 17, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/circresaha.116.309302 ;PMID: 28302739Full text available |
| 20 |
Material Type: Article
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Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism dataGenetics (Austin), 2011-09, Vol.189 (1), p.237-249 [Peer Reviewed Journal]Copyright Genetics Society of America Sep 2011 ;Copyright © 2011 by the Genetics Society of America 2011 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.111.130922 ;PMID: 21705750 ;CODEN: GENTAEFull text available |
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