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1
Clinical Characteristics and Surgical Outcomes of Turkish Patients With Pediatric Glaucoma Who Underwent Glaucoma Surgery in a University Hospital
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Clinical Characteristics and Surgical Outcomes of Turkish Patients With Pediatric Glaucoma Who Underwent Glaucoma Surgery in a University Hospital

Journal 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: 38112386

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2
Venous Tortuosity in COL4A2 -Associated Gould Syndrome
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Venous Tortuosity in COL4A2 -Associated Gould Syndrome

Ophthalmic 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: 10.3928/23258160-20230811-01

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3
Evaluation of chromosomal abnormalities in the postnatal cohort: A single‐center study on 14,242 patients
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Evaluation of chromosomal abnormalities in the postnatal cohort: A single‐center study on 14,242 patients

Journal 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: 38115218

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4
Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients
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Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients

Chromosoma, 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/s00412-022-00782-3

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5
Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil
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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil

Scientific 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: 36071085

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6
The Safety of Second-Generation Antipsychotics During Pregnancy: A Clinically Focused Review
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The Safety of Second-Generation Antipsychotics During Pregnancy: A Clinically Focused Review

CNS 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: 29637530

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7
Aplastic Anemia in Triple X Syndrome
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Aplastic Anemia in Triple X Syndrome

Children (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: 36670650

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8
Multi‐institutional experience of genetic diagnosis in Ecuador: National registry of chromosome alterations and polymorphisms
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Multi‐institutional experience of genetic diagnosis in Ecuador: National registry of chromosome alterations and polymorphisms

Molecular 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: 31830383

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9
SF3B1 mutant MDS-initiating cells may arise from the haematopoietic stem cell compartment
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SF3B1 mutant MDS-initiating cells may arise from the haematopoietic stem cell compartment

Nature 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: 26643973

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10
Serial Magnetic Resonance Imaging for Aortic Dilation in Tetralogy of Fallot With Pulmonary Stenosis
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Serial Magnetic Resonance Imaging for Aortic Dilation in Tetralogy of Fallot With Pulmonary Stenosis

The 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: 36669383

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11
Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders
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Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders

American 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: 33856167

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12
Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease
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Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease

Genes, 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: 35885957

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13
Hydrometrocolpos in Infants: Etiologies and Clinical Presentations
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Article
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Hydrometrocolpos in Infants: Etiologies and Clinical Presentations

Children (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: 35204939

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14
Effect of Prenatal Laterality Disturbance and Its Accompanying Anomalies on Survival
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Article
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Effect of Prenatal Laterality Disturbance and Its Accompanying Anomalies on Survival

The 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: 29954599

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15
Congenital heart disease and cardiac procedural outcomes in patients with trisomy 21 and Turner syndrome
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Article
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Congenital heart disease and cardiac procedural outcomes in patients with trisomy 21 and Turner syndrome

Congenital 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: 28736822

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16
Triple X Syndrome with a Rare Finding: Cleft Palate
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Article
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Triple X Syndrome with a Rare Finding: Cleft Palate

The 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.32154

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17
MicroRNA-4516 in Urinary Exosomes as a Biomarker of Premature Ovarian Insufficiency
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MicroRNA-4516 in Urinary Exosomes as a Biomarker of Premature Ovarian Insufficiency

Cells (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/cells11182797

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18
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 Gene
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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 Gene

Journal 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: 31782289

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19
Ultrasound Assessment of Larynx and Trachea in the Neonatal Period, Examination Standard with Predictive Values-Study Protocol
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Article
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Ultrasound Assessment of Larynx and Trachea in the Neonatal Period, Examination Standard with Predictive Values-Study Protocol

Diagnostics (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: 37174969

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20
The clinical impact of chromosomal microarray on paediatric care in Hong Kong
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The clinical impact of chromosomal microarray on paediatric care in Hong Kong

PloS 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: 25333781

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