Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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12th Fetal Cell Workshop: Prague, Czech Republic, May 12-13, 2001Fetal diagnosis and therapy, 2001-11, Vol.16 (6), p.437 [Peer Reviewed Journal]ISSN: 1015-3837 ;EISSN: 1421-9964Full text available |
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2 |
Material Type: Article
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12th Fetal Cell WorkshopFetal diagnosis and therapy, 2001-12, Vol.16 (6), p.437-464 [Peer Reviewed Journal]2001 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000053955Full text available |
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3 |
Material Type: Article
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15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring AnomaliesCase 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: 30538881Full text available |
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4 |
Material Type: Article
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15q23Gain in aNeonate with a GiantOmphaloceleandMiiltiple Co-Occurring AnomaliesCase reports in pediatrics, 2018-01, Vol.2018 [Peer Reviewed Journal]COPYRIGHT 2018 Hindawi Limited ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2018/8702568Full text available |
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5 |
Material Type: Article
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1963 Annual Meeting of the British Paediatric AssociationClinical pediatrics, 1963-09, Vol.2 (9), p.467-469 [Peer Reviewed Journal]ISSN: 0009-9228 ;EISSN: 1938-2707 ;DOI: 10.1177/000992286300200902Full text available |
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6 |
Material Type: Article
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2002 American Cytogenetic Conference Distinguished Cytogeneticist Award presented to Dr. Catherine PalmerCytogenetic and genome research, 2002-01, Vol.97 (3/4), p.261 [Peer Reviewed Journal]ISSN: 1424-8581 ;EISSN: 1424-859XFull text available |
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7 |
Material Type: Conference Proceeding
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2022 SPP Fall Meeting AbstractsPediatric and developmental pathology, 2022, Vol.25 (6), p.673-709 [Peer Reviewed Journal]2022, Society for Pediatric Pathology All rights reserved ;ISSN: 1093-5266 ;EISSN: 1615-5742 ;DOI: 10.1177/10935266221128365Digital Resources/Online E-Resources |
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8 |
Material Type: Article
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22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in BrazilAmerican journal of medical genetics. Part A, 2008-07, Vol.146A (13), p.1655-1661 [Peer Reviewed Journal]Copyright © 2008 Wiley‐Liss, Inc. ;2008 INIST-CNRS ;(c) 2008 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.32378 ;PMID: 18512234Full text available |
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9 |
Material Type: Article
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45,X/47,XXX Mosaicism and Short StatureCase reports in pediatrics, 2015-01, Vol.2015, p.263253-3 [Peer Reviewed Journal]Copyright © 2015 Erica Everest et al. ;Copyright © 2015 Erica Everest et al. Erica Everest et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2015 Erica Everest et al. 2015 ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2015/263253 ;PMID: 26137340Full text available |
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10 |
Material Type: Article
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45,X mosaicism in northeast China: a clinical report and review of the literatureJournal of assisted reproduction and genetics, 2013-03, Vol.30 (3), p.407-412 [Peer Reviewed Journal]The Author(s) 2013 ;Springer Science+Business Media New York 2013 ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-012-9927-3 ;PMID: 23299637Full text available |
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11 |
Material Type: Article
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48,XYYY: A Rare Case ReportBalkan journal of medical genetics, 2022-06, Vol.24 (2), p.103-106 [Peer Reviewed Journal]2021. 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: 1311-0160 ;EISSN: 2199-5761 ;DOI: 10.2478/bjmg-2021-0029Full text available |
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12 |
Material Type: Article
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630. Hydatidiform mole; trophoblastic disease not otherwise statedIncidence and Prevalence Data, 2010-04Copyright Timely Data Resources, Inc. Second Quarter 2010Digital Resources/Online E-Resources |
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13 |
Material Type: Article
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630. Hydatidiform mole; trophoblastic disease not otherwise statedIncidence and Prevalence Data, 2013-01Copyright Timely Data Resources, Inc. First Quarter 2013Digital Resources/Online E-Resources |
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14 |
Material Type: Article
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630. Hydatidiform mole; trophoblastic disease not otherwise statedIncidence and Prevalence Data, 2011-01Copyright Timely Data Resources, Inc. First Quarter 2011Digital Resources/Online E-Resources |
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15 |
Material Type: Article
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758.6 Gonadal dysgenesis; Turner syndrome (45,X); XO syndromeIncidence and Prevalence Data, 2011-04Copyright Timely Data Resources, Inc. Second Quarter 2011Digital Resources/Online E-Resources |
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16 |
Material Type: Article
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758.6 Gonadal dysgenesis; Turner syndrome (45,X); XO syndromeIncidence and Prevalence Data, 2010-04Copyright Timely Data Resources, Inc. Second Quarter 2010Digital Resources/Online E-Resources |
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17 |
Material Type: Article
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758.6 Gonadal dysgenesis; Turner syndrome (45,X); XO syndromeIncidence and Prevalence Data, 2012-01Copyright Timely Data Resources, Inc. First Quarter 2012Digital Resources/Online E-Resources |
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18 |
Material Type: Article
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758.6 Gonadal dysgenesis; Turner syndrome (45,X); XO syndromeIncidence and Prevalence Data, 2009-10Copyright Timely Data Resources, Inc. Fourth Quarter 2009Digital Resources/Online E-Resources |
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19 |
Material Type: Article
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758.8 Other conditions due to sex chromosome anomaliesIncidence and Prevalence Data, 2011-07Copyright Timely Data Resources, Inc. Third Quarter 2011Digital Resources/Online E-Resources |
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20 |
Material Type: Article
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758.8 Other conditions due to sex chromosome anomaliesIncidence and Prevalence Data, 2010-01Copyright Timely Data Resources, Inc. First Quarter 2010Digital Resources/Online E-Resources |