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Material Type: Article
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Diploid/triploid mosaicism: a variable but characteristic phenotypeRevista de neurologiá, 2014-08, Vol.59 (4), p.158-163 [Peer Reviewed Journal]EISSN: 1576-6578 ;DOI: 10.33588/rn.5904.2014077 ;PMID: 25059266Full text available |
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Placental mesenchymal dysplasiaArchives of pathology & laboratory medicine (1976), 2007-01, Vol.131 (1), p.131-137 [Peer Reviewed Journal]COPYRIGHT 2007 College of American Pathologists ;Copyright College of American Pathologists Jan 2007 ;ISSN: 0003-9985 ;ISSN: 1543-2165 ;EISSN: 1543-2165 ;DOI: 10.5858/2007-131-131-pmd ;PMID: 17227114 ;CODEN: APLMASFull text available |
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Material Type: Article
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Triploidy in a growth discordant twin pregnancy after intracytoplasmic sperm injection treatment : Case reportFetal diagnosis and therapy, 2006-01, Vol.21 (1), p.65-67 [Peer Reviewed Journal]2006 INIST-CNRS ;(c) 2006 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000089050 ;PMID: 16354978Full text available |
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Invited Commentary: Intermittent Opioid Use and Ischemic Placental Disease—Clarifying Associations With Adverse Pregnancy OutcomesAmerican journal of epidemiology, 2022-03, Vol.191 (5), p.769-772 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. ;ISSN: 0002-9262 ;EISSN: 1476-6256 ;DOI: 10.1093/aje/kwab225 ;PMID: 34528062Full text available |
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Material Type: Article
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A review of trisomy X (47,XXX)Orphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Peer Reviewed Journal]COPYRIGHT 2010 BioMed Central Ltd. ;COPYRIGHT 2010 BioMed Central Ltd. ;Copyright ©2010 Tartaglia et al; licensee BioMed Central Ltd. 2010 Tartaglia et al; licensee BioMed Central Ltd. ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/1750-1172-5-8 ;PMID: 20459843Full text available |
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Material Type: Article
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Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformationsScientific reports, 2024-04, Vol.14 (1), p.9220-9220 [Peer Reviewed Journal]2024. The Author(s). ;The Author(s) 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. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-59422-8 ;PMID: 38649697Full text available |
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Material Type: Article
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovariesClinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Peer Reviewed Journal]2019 The Authors. published by John Wiley & Sons Ltd. ;2019. 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: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.2207 ;PMID: 31183102Full text available |
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Material Type: Article
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Genetic and Clinical Features of Triploid Fetus: A Case Report in Han Chinese PopulationPakistan journal of zoology, 2015-04, Vol.47 (2) [Peer Reviewed Journal]COPYRIGHT 2015 Knowledge Bylanes ;ISSN: 0030-9923Full text available |
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9 |
Material Type: Article
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Turner syndrome and 45,X/47,XXX mosaicismGenetic counseling, 2009-01, Vol.20 (2), p.141-146 [Peer Reviewed Journal]Copyright Éditions Médecine et Hygiène 2009 ;ISSN: 1015-8146 ;PMID: 19650411Full text available |
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10 |
Material Type: Article
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Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experienceBMC pregnancy and childbirth, 2023-01, Vol.23 (1), p.73-73, Article 73 [Peer Reviewed Journal]2023. The Author(s). ;2023. 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) 2023 ;ISSN: 1471-2393 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-023-05394-y ;PMID: 36703098Full text available |
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An unusual case of trisomy and triploidy in a chorion villus biopsyPrenatal diagnosis, 2000-11, Vol.20 (11), p.917-920 [Peer Reviewed Journal]Copyright © 2000 John Wiley & Sons, Ltd. ;2001 INIST-CNRS ;Copyright 2000 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200011)20:11<917::AID-PD937>3.0.CO;2-9 ;PMID: 11113896 ;CODEN: PRDIDMFull text available |
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12 |
Material Type: Article
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Craniofacial and dental manifestations of triple X syndrome associated with congenital hypothyroidism: a case reportSpecial care in dentistry, 2014-05, Vol.34 (3), p.156-159 [Peer Reviewed Journal]2013 Special Care Dentistry Association and Wiley Periodicals, Inc. ;ISSN: 0275-1879 ;EISSN: 1754-4505 ;DOI: 10.1111/scd.12050 ;PMID: 24117978Full text available |
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13 |
Material Type: Article
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The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteriaJournal of medical genetics, 1999-11, Vol.36 (11), p.837-842 [Peer Reviewed Journal]Journal of Medical Genetics ;1999 INIST-CNRS ;Copyright: 1999 Journal of Medical Genetics ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.36.11.837 ;PMID: 10544228 ;CODEN: JMDGAEFull text available |
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14 |
Material Type: Article
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Genetic counseling for sex chromosome abnormalitiesAmerican journal of medical genetics, 2002-06, Vol.110 (1), p.3-10 [Peer Reviewed Journal]Copyright © 2002 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2002 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.10391 ;PMID: 12116264 ;CODEN: AJMGDAFull text available |
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Material Type: Article
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Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnanciesBJOG : an international journal of obstetrics and gynaecology, 2012-04, Vol.119 (5), p.614-625 [Peer Reviewed Journal]2012 The Authors BJOG An International Journal of Obstetrics and Gynaecology © 2012 RCOG ;2015 INIST-CNRS ;2012 The Authors BJOG An International Journal of Obstetrics and Gynaecology © 2012 RCOG. ;ISSN: 1470-0328 ;EISSN: 1471-0528 ;DOI: 10.1111/j.1471-0528.2012.03279.x ;PMID: 22313859 ;CODEN: BIOGFQFull text available |
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16 |
Material Type: Article
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Fetal axillary cystic hygroma: A novel association with triple X syndromeBirth defects research. A Clinical and molecular teratology, 2012-11, Vol.94 (11), p.955-957 [Peer Reviewed Journal]Copyright © 2012 Wiley Periodicals, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.23083 ;PMID: 23109196Full text available |
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Material Type: Article
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Genomic imprinting in the development and evolution of psychotic spectrum conditionsBiological reviews of the Cambridge Philosophical Society, 2008-11, Vol.83 (4), p.441-493 [Peer Reviewed Journal]2008 The Author Journal compilation © 2008 Cambridge Philosophical Society ;ISSN: 1464-7931 ;EISSN: 1469-185X ;DOI: 10.1111/j.1469-185X.2008.00050.x ;PMID: 18783362 ;CODEN: BRCPAHFull text available |
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18 |
Material Type: Article
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Combined diagnosis of QF‐PCR and CNV‐Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosisJournal 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: 35195919Full text available |
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19 |
Material Type: Article
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Growth Retardation in Turner Syndrome: Aneuploidy, Rather Than Specific Gene Loss, May Explain Growth FailureThe journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4578-4582 [Peer Reviewed Journal]ISSN: 0021-972X ;EISSN: 1945-7197 ;DOI: 10.1210/jcem.84.12.6200Full text available |
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20 |
Material Type: Article
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Triple X syndrome: a review of the literatureEuropean journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.265-271 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright Nature Publishing Group Mar 2010 ;Copyright © 2010 Macmillan Publishers Limited 2010 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2009.109 ;PMID: 19568271Full text available |