Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Article
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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, p.1-10 [Peer Reviewed Journal]COPYRIGHT 2023 Slack, Inc. ;Copyright 2023, 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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Material Type: Article
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Venous Tortuosity in COL4A2 -Associated Gould SyndromeOphthalmic surgery, lasers & imaging, 2023-09, Vol.54 (9), p.536-539 [Peer Reviewed Journal]COPYRIGHT 2023 Slack, Inc. ;Copyright 2023, SLACK Incorporated ;ISSN: 2325-8160 ;EISSN: 2325-8179 ;EISSN: 1938-2375 ;DOI: 10.3928/23258160-20230811-01Full text available |
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Material Type: Article
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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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Material Type: Article
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Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patientsChromosoma, 2022-12, Vol.131 (4), p.225-237 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;ISSN: 0009-5915 ;EISSN: 1432-0886 ;DOI: 10.1007/s00412-022-00782-3Full text available |
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Material Type: Article
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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in BrazilScientific reports, 2022-09, Vol.12 (1), p.15184-15184, Article 15184 [Peer Reviewed Journal]The Author(s) 2022. 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. ;The Author(s) 2022 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-022-19274-6 ;PMID: 36071085Full text available |
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Material Type: Article
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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 |
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Material Type: Article
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Aplastic Anemia in Triple X SyndromeChildren (Basel), 2023-01, Vol.10 (1), p.100 [Peer Reviewed Journal]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: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children10010100 ;PMID: 36670650Full text available |
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8 |
Material Type: Article
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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 |
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9 |
Material Type: Article
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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 |
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10 |
Material Type: Article
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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 |
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11 |
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 |
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12 |
Material Type: Article
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Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart DiseaseGenes, 2022-06, Vol.13 (7), p.1172 [Peer Reviewed Journal]COPYRIGHT 2022 MDPI AG ;2022 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. ;2022 by the authors. 2022 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes13071172 ;PMID: 35885957Full text available |
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13 |
Material Type: Article
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Hydrometrocolpos in Infants: Etiologies and Clinical PresentationsChildren (Basel), 2022-02, Vol.9 (2), p.219 [Peer Reviewed Journal]2022 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. ;2022 by the authors. 2022 ;ISSN: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children9020219 ;PMID: 35204939Full text available |
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Material Type: Article
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Effect of Prenatal Laterality Disturbance and Its Accompanying Anomalies on SurvivalThe American journal of cardiology, 2018-08, Vol.122 (4), p.663-671 [Peer Reviewed Journal]2018 Elsevier Inc. ;Copyright © 2018 Elsevier Inc. All rights reserved. ;2018. Elsevier Inc. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2018.04.040 ;PMID: 29954599Full text available |
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15 |
Material Type: Article
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Congenital heart disease and cardiac procedural outcomes in patients with trisomy 21 and Turner syndromeCongenital heart disease, 2017-11, Vol.12 (6), p.820-827 [Peer Reviewed Journal]2017 Wiley Periodicals, Inc. ;ISSN: 1747-079X ;EISSN: 1747-0803 ;DOI: 10.1111/chd.12521 ;PMID: 28736822Full text available |
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16 |
Material Type: Article
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Triple X Syndrome with a Rare Finding: Cleft PalateThe journal of pediatric research, 2018-06, Vol.5 (2), p.100-102 [Peer Reviewed Journal]COPYRIGHT 2018 Galenos Yayinevi Tic. Ltd. ;2018. This work is published under https://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: 2147-9445 ;EISSN: 2147-9445 ;EISSN: 2587-2478 ;DOI: 10.4274/jpr.32154Full text available |
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17 |
Material Type: Article
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MicroRNA-4516 in Urinary Exosomes as a Biomarker of Premature Ovarian InsufficiencyCells (Basel, Switzerland), 2022-09, Vol.11 (18), p.2797 [Peer Reviewed Journal]COPYRIGHT 2022 MDPI AG ;2022 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. ;2022 by the authors. 2022 ;ISSN: 2073-4409 ;EISSN: 2073-4409 ;DOI: 10.3390/cells11182797Full text available |
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18 |
Material Type: Article
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Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 GeneJournal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.319-328 [Peer Reviewed Journal]2020. This work is published under https://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. ;Copyright 2020 by Turkish Pediatric Endocrinology and Diabetes Society | The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House. 2020 ;ISSN: 1308-5727 ;EISSN: 1308-5735 ;DOI: 10.4274/jcrpe.galenos.2019.2019.0142 ;PMID: 31782289Full text available |
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Material Type: Article
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Ultrasound Assessment of Larynx and Trachea in the Neonatal Period, Examination Standard with Predictive Values-Study ProtocolDiagnostics (Basel), 2023-04, Vol.13 (9), p.1578 [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: 2075-4418 ;EISSN: 2075-4418 ;DOI: 10.3390/diagnostics13091578 ;PMID: 37174969Full text available |
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Material Type: Article
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The clinical impact of chromosomal microarray on paediatric care in Hong KongPloS one, 2014-10, Vol.9 (10), p.e109629-e109629 [Peer Reviewed Journal]COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Tao 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. ;2014 Tao et al 2014 Tao et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0109629 ;PMID: 25333781Full text available |