Results 1 - 20 of 48 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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Clinical Characteristics and Surgical Outcomes of Turkish Patients With Pediatric Glaucoma Who Underwent Glaucoma Surgery in a University HospitalJournal of pediatric ophthalmology and strabismus, 2023-12, Vol.61 (3), p.188-10 [Peer Reviewed Journal]COPYRIGHT 2023 Slack, Inc. ;Copyright 2023, SLACK Incorporated ;Copyright 2024, SLACK Incorporated ;ISSN: 0191-3913 ;ISSN: 0022-0124 ;EISSN: 1938-2405 ;EISSN: 1938-2472 ;DOI: 10.3928/01913913-20231026-04 ;PMID: 38112386Full text available |
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Contact endoscopic findings in hereditary hemorrhagic telangiectasiaHead & neck, 2006-01, Vol.28 (1), p.56-63 [Peer Reviewed Journal]Copyright © 2005 Wiley Periodicals, Inc. ;2006 INIST-CNRS ;(c) 2005 Wiley Periodicals, Inc. Head Neck 27: XXX-XXX, 2005. ;ISSN: 1043-3074 ;EISSN: 1097-0347 ;DOI: 10.1002/hed.20300 ;PMID: 16302189Full text available |
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Transporting babies with known heart disease; who, what and where?Archives of disease in childhood. Fetal and neonatal edition, 2007-03, Vol.92 (2), p.F80-F81 [Peer Reviewed Journal]Copyright 2007 Archives of Disease in Childhood ;Copyright: 2007 Copyright 2007 Archives of Disease in Childhood ;Copyright ©2007 BMJ Publishing Group & Royal College of Paediatrics and Child Health ;ISSN: 1359-2998 ;EISSN: 1468-2052 ;DOI: 10.1136/adc.2006.101626 ;PMID: 17337670Full text available |
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Morbidity in 47,XYY syndrome: a nationwide epidemiological study of hospital diagnoses and medication useGenetics in medicine, 2020-09, Vol.22 (9), p.1542-1551 [Peer Reviewed Journal]American College of Medical Genetics and Genomics 2020. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-0837-y ;PMID: 32475987Full text available |
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Turner syndrome: mechanisms and managementNature reviews. Endocrinology, 2019-10, Vol.15 (10), p.601-614 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2019 ;ISSN: 1759-5029 ;EISSN: 1759-5037 ;DOI: 10.1038/s41574-019-0224-4 ;PMID: 31213699Full text available |
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Evaluation of chromosomal abnormalities in the postnatal cohort: A single‐center study on 14,242 patientsJournal of clinical laboratory analysis, 2024-01, Vol.38 (1-2), p.e24997-n/a [Peer Reviewed Journal]2023 The Authors. published by Wiley Periodicals LLC. ;2023 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. ;2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.24997 ;PMID: 38115218Full text available |
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TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndromePLoS genetics, 2018-10, Vol.14 (10), p.e1007692-e1007692 [Peer Reviewed Journal]COPYRIGHT 2018 Public Library of Science ;2018 Corbitt et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018 Corbitt et al 2018 Corbitt et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1007692 ;PMID: 30281655Full text available |
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The Safety of Second-Generation Antipsychotics During Pregnancy: A Clinically Focused ReviewCNS drugs, 2018-04, Vol.32 (4), p.351-366 [Peer Reviewed Journal]Springer International Publishing AG, part of Springer Nature 2018 ;Copyright Springer Science & Business Media Apr 2018 ;ISSN: 1172-7047 ;EISSN: 1179-1934 ;DOI: 10.1007/s40263-018-0517-5 ;PMID: 29637530Full text available |
| 9 |
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The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosisJournal of clinical laboratory analysis, 2020-12, Vol.34 (12), p.e23514-n/a [Peer Reviewed Journal]2020 The Authors. Published by Wiley Periodicals LLC ;2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals LLC. ;2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.23514 ;PMID: 32864771Full text available |
| 10 |
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Organ Abnormalities Caused by Turner SyndromeCells (Basel, Switzerland), 2023-05, Vol.12 (10), p.1365 [Peer Reviewed Journal]COPYRIGHT 2023 MDPI AG ;2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 2073-4409 ;EISSN: 2073-4409 ;DOI: 10.3390/cells12101365 ;PMID: 37408200Full text available |
| 11 |
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Understanding the interaction between cytomegalovirus and tuberculosis in children: The way forwardPLoS pathogens, 2021-12, Vol.17 (12), p.e1010061-e1010061 [Peer Reviewed Journal]COPYRIGHT 2021 Public Library of Science ;2021 Olbrich et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 Olbrich et al 2021 Olbrich et al ;ISSN: 1553-7374 ;ISSN: 1553-7366 ;EISSN: 1553-7374 ;DOI: 10.1371/journal.ppat.1010061 ;PMID: 34882748Full text available |
| 12 |
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HILIC-UPLC-MS for high throughput and isomeric N-glycan separation and characterization in Congenital Disorders Glycosylation and human diseasesGlycoconjugate journal, 2021-04, Vol.38 (2), p.201-211 [Peer Reviewed Journal]Springer Science+Business Media, LLC, part of Springer Nature 2020 ;COPYRIGHT 2021 Springer ;Springer Science+Business Media, LLC, part of Springer Nature 2020. ;ISSN: 0282-0080 ;EISSN: 1573-4986 ;DOI: 10.1007/s10719-020-09947-7 ;PMID: 32915358Full text available |
| 13 |
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The Genomic Architecture of Bladder Exstrophy Epispadias ComplexGenes, 2021-07, Vol.12 (8), p.1149 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12081149 ;PMID: 34440323Full text available |
| 14 |
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Primary Amenorrhea Due to Anatomical Abnormalities of the Reproductive Tract: Molecular InsightInternational journal of molecular sciences, 2021-10, Vol.22 (21), p.11495 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms222111495 ;PMID: 34768925Full text available |
| 15 |
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Multi‐institutional experience of genetic diagnosis in Ecuador: National registry of chromosome alterations and polymorphismsMolecular genetics & genomic medicine, 2020-02, Vol.8 (2), p.e1087-n/a [Peer Reviewed Journal]2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2020. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1087 ;PMID: 31830383Full text available |
| 16 |
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SF3B1 mutant MDS-initiating cells may arise from the haematopoietic stem cell compartmentNature communications, 2015-12, Vol.6 (1), p.10004, Article 10004 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2015 ;Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2015 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms10004 ;PMID: 26643973Full text available |
| 17 |
Material Type: Article
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Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum DisordersAmerican family physician, 2021-04, Vol.103 (8), p.481-492 [Peer Reviewed Journal]COPYRIGHT 2021 American Academy of Family Physicians ;Copyright American Academy of Family Physicians Apr 15, 2021 ;ISSN: 0002-838X ;EISSN: 1532-0650 ;PMID: 33856167Full text available |
| 18 |
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Serial Magnetic Resonance Imaging for Aortic Dilation in Tetralogy of Fallot With Pulmonary StenosisThe American journal of cardiology, 2023-03, Vol.191, p.92-100 [Peer Reviewed Journal]2022 Elsevier Inc. ;Copyright © 2022 Elsevier Inc. All rights reserved. ;2022. Elsevier Inc. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2022.12.015 ;PMID: 36669383Full text available |
| 19 |
Material Type: Article
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Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactylyGenetics in medicine, 2021-04, Vol.23 (4), p.679-688 [Peer Reviewed Journal]2021 The Author(s) ;The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics 2021. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-01052-2 ;PMID: 33442026Full text available |
| 20 |
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Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome casesGenome medicine, 2019-05, Vol.11 (1), p.30-30, Article 30 [Peer Reviewed Journal]COPYRIGHT 2019 BioMed Central Ltd. ;2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s). 2019 ;ISSN: 1756-994X ;EISSN: 1756-994X ;DOI: 10.1186/s13073-019-0639-5 ;PMID: 31101064Full text available |
Results 1 - 20 of 48 for All Library Resources
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