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Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening
Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening
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Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening

Journal of clinical laboratory analysis, 2020-08, Vol.34 (8), p.e23347-n/a [Peer Reviewed Journal]

2020 The Authors. Published by Wiley Periodicals, Inc. ;2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc. ;2020. 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.23347 ;PMID: 32342531

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2
Hydrometrocolpos in Infants: Etiologies and Clinical Presentations
Hydrometrocolpos in Infants: Etiologies and Clinical Presentations
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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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3
Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities
Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities
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Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.725-730 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2013 ;Copyright © 2013 Macmillan Publishers Limited 2013 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2012.253 ;PMID: 23211699

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4
Combined diagnosis of QF‐PCR and CNV‐Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosis
Combined diagnosis of QF‐PCR and CNV‐Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosis
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Combined diagnosis of QF‐PCR and CNV‐Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosis

Journal of clinical laboratory analysis, 2022-04, Vol.36 (4), p.e24311-n/a [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC ;2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. ;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. ;ISSN: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.24311 ;PMID: 35195919

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5
Triple X Syndrome with a Rare Finding: Cleft Palate
Triple X Syndrome with a Rare Finding: Cleft Palate
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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: 2587-2478 ;EISSN: 2147-9445 ;DOI: 10.4274/jpr.32154

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6
Pregnancy Outcomes of Non-Visualization of the Fetal Gallbladder from a Chinese Tertiary Single Centre and Literature Review
Pregnancy Outcomes of Non-Visualization of the Fetal Gallbladder from a Chinese Tertiary Single Centre and Literature Review
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Pregnancy Outcomes of Non-Visualization of the Fetal Gallbladder from a Chinese Tertiary Single Centre and Literature Review

Children (Basel), 2022-08, Vol.9 (9), p.1288 [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: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children9091288

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7
Fontaine progeroid syndrome—A case report
Fontaine progeroid syndrome—A case report
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Fontaine progeroid syndrome—A case report

Clinical case reports, 2022-09, Vol.10 (9), p.n/a [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd. ;2022. 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: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.6291 ;PMID: 36093452

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8
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies
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15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies

Case reports in pediatrics, 2018-01, Vol.2018, p.8702568-5 [Peer Reviewed Journal]

Copyright © 2018 Hui-Fang Zhou et al. ;Copyright © 2018 Hui-Fang Zhou et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2018 Hui-Fang Zhou et al. 2018 ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2018/8702568 ;PMID: 30538881

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9
Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli’s disease)
Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli’s disease)
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Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli’s disease)

Gut, 1999-11, Vol.45 (5), p.780-782 [Peer Reviewed Journal]

British Society of Gastroenterology ;1999 INIST-CNRS ;Copyright: 1999 British Society of Gastroenterology ;ISSN: 0017-5749 ;ISSN: 1468-3288 ;EISSN: 1468-3288 ;DOI: 10.1136/gut.45.5.780 ;PMID: 10517920 ;CODEN: GUTTAK

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