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Refined by: subject: Heart Defects, Congenital - Genetics

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1	Material Type: Article	Risk factors for conotruncal cardiac defects in Atlanta Journal of the American College of Cardiology, 1989-08, Vol.14 (2), p.432-442 [Peer Reviewed Journal] 1989 ;1989 INIST-CNRS ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/0735-1097(89)90199-X ;PMID: 2787814 ;CODEN: JACCDI Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	Material Type: Article	Neutrophil oxidative metabolism in Down syndrome patients with congenital heart defects Environmental and molecular mutagenesis, 2010, Vol.51 (1), p.57-63 [Peer Reviewed Journal] Copyright © 2009 Wiley‐Liss, Inc. ;2015 INIST-CNRS ;(c) 2009 Wiley-Liss, Inc. ;ISSN: 0893-6692 ;EISSN: 1098-2280 ;DOI: 10.1002/em.20511 ;PMID: 19593803 ;CODEN: EMMUEG Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
3	Material Type: Article	Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt-oram and ulnar-mammary syndromes American journal of medical genetics. Part A, 2013-07, Vol.161A (7), p.1797-1802 [Peer Reviewed Journal] Copyright © 2013 Wiley Periodicals, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.36054 ;PMID: 23713051 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture Genes & development, 1997-12, Vol.11 (23), p.3143-3156 [Peer Reviewed Journal] Copyright © 1997, Cold Spring Harbor Laboratory Press 1997 ;ISSN: 0890-9369 ;EISSN: 1549-5477 ;DOI: 10.1101/gad.11.23.3143 ;PMID: 9389647 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations Orphanet journal of rare diseases, 2013-06, Vol.8 (1), p.84-84 [Peer Reviewed Journal] 2013 Banka and Newman; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2013 Banka and Newman; licensee BioMed Central Ltd. 2013 Banka and Newman; licensee BioMed Central Ltd. ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/1750-1172-8-84 ;PMID: 23758768 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
6	Material Type: Article	Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms Birth defects research, 2018-12, Vol.110 (20), p.1504 2018 Wiley Periodicals, Inc. ;EISSN: 2472-1727 ;DOI: 10.1002/bdr2.1435 ;PMID: 30576094 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
7	Material Type: Article	Risk factors for the development of congenital heart defects in children born in the Tuzla Canton Medicinski arhiv, 2002, Vol.56 (2), p.73 PMID: 12014099 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
8	Material Type: Article	Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure BMC genetics, 2012-11, Vol.13 (1), p.104-104, Article 104 [Peer Reviewed Journal] 2012 Bendon et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2012 Bendon et al.; licensee BioMed Central Ltd. 2012 Bendon et al.; licensee BioMed Central Ltd. ;ISSN: 1471-2350 ;ISSN: 1471-2156 ;EISSN: 1471-2350 ;EISSN: 1471-2156 ;DOI: 10.1186/1471-2350-13-104 ;PMID: 23140272 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Prenatal Cardiovascular Adaptation Advances in experimental medicine and biology, 1972, Vol.22, p.3-11 [Peer Reviewed Journal] Plenum Press, New York 1972 ;ISSN: 0065-2598 ;ISBN: 146843215X ;ISBN: 9781468432152 ;EISSN: 2214-8019 ;EISBN: 1468432133 ;EISBN: 9781468432138 ;DOI: 10.1007/978-1-4684-3213-8_1 ;PMID: 5074648 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
10	Material Type: Article	The geneticist's role in adult congenital heart disease Cardiology clinics, 2006-11, Vol.24 (4), p.557 [Peer Reviewed Journal] ISSN: 0733-8651 ;EISSN: 1558-2264 ;DOI: 10.1016/j.ccl.2006.08.001 ;PMID: 17098511 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
11	Material Type: Article	Incidence, nature and etiology of malformations of the heart in man Proceedings of the Royal Society of Medicine, 1974-05, Vol.67 (5), p.353-354 ISSN: 0035-9157 ;DOI: 10.1177/003591577406700511 ;PMID: 4835280 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	Familial total anomalous pulmonary venous return: A large Utah-Idaho family American journal of medical genetics, 1994-10, Vol.52 (4), p.462-466 [Peer Reviewed Journal] Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company ;1995 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320520412 ;PMID: 7747759 ;CODEN: AJMGDA Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
13	Material Type: Article	Congenital heart disease: current knowledge about causes and inheritance Medical journal of Australia, 2012-08, Vol.197 (3), p.155 [Peer Reviewed Journal] EISSN: 1326-5377 ;DOI: 10.5694/mja12.10811 ;PMID: 22860792 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
14	Material Type: Article	Targeted next generation sequencing of a panel of autism-related genes identifies an EHMT1 mutation in a Kleefstra syndrome patient with autism and normal intellectual performance Gene, 2016-12, Vol.595 (2), p.131 [Peer Reviewed Journal] Copyright © 2016 Elsevier B.V. All rights reserved. ;EISSN: 1879-0038 ;DOI: 10.1016/j.gene.2016.09.027 ;PMID: 27651234 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
15	Material Type: Article	Congenital heart malformations: aetiology and associations Seminars in neonatology, 2001-02, Vol.6 (1), p.17-25 2001 Harcourt Publishers Ltd ;2001 INIST-CNRS ;Copyright 2001 Harcourt Publishers Ltd. ;ISSN: 1084-2756 ;EISSN: 1532-2815 ;DOI: 10.1053/siny.2000.0032 ;PMID: 11162282 ;CODEN: SNEOFI Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	Common molecular causes for congenital heart defects and microcephaly American journal of obstetrics and gynecology, 2010-02, Vol.202 (2), p.e7; author reply e7 [Peer Reviewed Journal] EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2009.08.034 ;PMID: 19804876 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
17	Material Type: Article	Genetic aspects of heart disease in the newborn Seminars in perinatology, 1993-04, Vol.17 (2), p.61 [Peer Reviewed Journal] ISSN: 0146-0005 ;EISSN: 1558-075X ;PMID: 8327904 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
18	Material Type: Article	Causes of malformations of the heart BMJ, 1965-10, Vol.2 (5467), p.895-904 [Peer Reviewed Journal] Copyright BMJ Publishing Group LTD Oct 16, 1965 ;ISSN: 0007-1447 ;ISSN: 0959-8138 ;EISSN: 1468-5833 ;DOI: 10.1136/bmj.2.5467.895 ;PMID: 5831199 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	Non-compaction cardiomyopathy: prevalence, prognosis, pathoetiology, genetics, and risk of cardioembolism Current heart failure reports, 2014-12, Vol.11 (4), p.393 [Peer Reviewed Journal] EISSN: 1546-9549 ;DOI: 10.1007/s11897-014-0227-3 ;PMID: 25239435 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
20	Material Type: Article	Etiology of congenital cardiopathies and genetic counseling Soins. Cardiologie, 1984-04 (14), p.15 ISSN: 0755-1916 ;PMID: 6563754 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by

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Results 1 - 20 of 151 for All Library Resources

1989 ;1989 INIST-CNRS ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/0735-1097(89)90199-X ;PMID: 2787814 ;CODEN: JACCDI

Copyright © 2009 Wiley‐Liss, Inc. ;2015 INIST-CNRS ;(c) 2009 Wiley-Liss, Inc. ;ISSN: 0893-6692 ;EISSN: 1098-2280 ;DOI: 10.1002/em.20511 ;PMID: 19593803 ;CODEN: EMMUEG

Copyright © 2013 Wiley Periodicals, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.36054 ;PMID: 23713051

Copyright © 1997, Cold Spring Harbor Laboratory Press 1997 ;ISSN: 0890-9369 ;EISSN: 1549-5477 ;DOI: 10.1101/gad.11.23.3143 ;PMID: 9389647

2018 Wiley Periodicals, Inc. ;EISSN: 2472-1727 ;DOI: 10.1002/bdr2.1435 ;PMID: 30576094

PMID: 12014099

Plenum Press, New York 1972 ;ISSN: 0065-2598 ;ISBN: 146843215X ;ISBN: 9781468432152 ;EISSN: 2214-8019 ;EISBN: 1468432133 ;EISBN: 9781468432138 ;DOI: 10.1007/978-1-4684-3213-8_1 ;PMID: 5074648

ISSN: 0733-8651 ;EISSN: 1558-2264 ;DOI: 10.1016/j.ccl.2006.08.001 ;PMID: 17098511

ISSN: 0035-9157 ;DOI: 10.1177/003591577406700511 ;PMID: 4835280

Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company ;1995 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320520412 ;PMID: 7747759 ;CODEN: AJMGDA

EISSN: 1326-5377 ;DOI: 10.5694/mja12.10811 ;PMID: 22860792

Copyright © 2016 Elsevier B.V. All rights reserved. ;EISSN: 1879-0038 ;DOI: 10.1016/j.gene.2016.09.027 ;PMID: 27651234

2001 Harcourt Publishers Ltd ;2001 INIST-CNRS ;Copyright 2001 Harcourt Publishers Ltd. ;ISSN: 1084-2756 ;EISSN: 1532-2815 ;DOI: 10.1053/siny.2000.0032 ;PMID: 11162282 ;CODEN: SNEOFI

EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2009.08.034 ;PMID: 19804876

ISSN: 0146-0005 ;EISSN: 1558-075X ;PMID: 8327904

Copyright BMJ Publishing Group LTD Oct 16, 1965 ;ISSN: 0007-1447 ;ISSN: 0959-8138 ;EISSN: 1468-5833 ;DOI: 10.1136/bmj.2.5467.895 ;PMID: 5831199

EISSN: 1546-9549 ;DOI: 10.1007/s11897-014-0227-3 ;PMID: 25239435

ISSN: 0755-1916 ;PMID: 6563754

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