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1
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1279 ;PMID: 32463164

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2
Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus
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Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus

Archives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Peer Reviewed Journal]

Springer-Verlag Berlin Heidelberg 2013 ;Archives of Gynecology and Obstetrics is a copyright of Springer, (2013). All Rights Reserved. ;ISSN: 0932-0067 ;EISSN: 1432-0711 ;DOI: 10.1007/s00404-013-2847-3 ;PMID: 23625330

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3
TRIPLOIDÍA 69,XXX EN RELACIÓN A LA EXPOSICIÓN PATERNA AL FINASTERIDE
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TRIPLOIDÍA 69,XXX EN RELACIÓN A LA EXPOSICIÓN PATERNA AL FINASTERIDE

BAG. Journal of basic and applied genetics, 2017-01, Vol.28, p.119 [Peer Reviewed Journal]

ISSN: 1666-0390 ;EISSN: 1852-6233

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4
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study

Orphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 2019. 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). 2019 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-018-0976-2 ;PMID: 30642344

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5
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study

Prenatal diagnosis, 2016-06, Vol.36 (6), p.523-529 [Peer Reviewed Journal]

2016 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4817 ;PMID: 27018091

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6
45,X/47,XXX Mosaicism and Short Stature
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45,X/47,XXX Mosaicism and Short Stature

Case 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: 26137340

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7
Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester
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Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester

Fetal diagnosis and therapy, 2000-03, Vol.15 (2), p.97-101 [Peer Reviewed Journal]

2000 S. Karger AG, Basel ;2000 INIST-CNRS ;Copyright 2000 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874

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8
Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases

Prenatal diagnosis, 2004-12, Vol.24 (12), p.1020-1021 [Peer Reviewed Journal]

Copyright © 2004 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1047 ;PMID: 15614873

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9
Diagnóstico prenatal de un feto con doble trisomía con cariotipo 48 XXX +18: reporte de un caso
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Diagnóstico prenatal de un feto con doble trisomía con cariotipo 48 XXX +18: reporte de un caso

Ginecologia y obstetricia de Mexico, 2018-12, Vol.86 (12), p.810-814

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0300-9041 ;DOI: 10.24245/gom.v86i12.1814

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10
Management of Pregnancy Achieved by Oocyte Donation to a Woman with 47,XXX and POF
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Management of Pregnancy Achieved by Oocyte Donation to a Woman with 47,XXX and POF

Journal of mammalian ova research, 2011-10, Vol.28 (3), p.139-142

ISSN: 1341-7738 ;EISSN: 1347-5878 ;DOI: 10.1274/jmor.28.139

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11
Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX
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Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX

The journal of obstetrics and gynaecology research, 2014-01, Vol.40 (1), p.259-262 [Peer Reviewed Journal]

2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology ;2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology. ;ISSN: 1341-8076 ;EISSN: 1447-0756 ;DOI: 10.1111/jog.12131 ;PMID: 23937348

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12
Long-term survival in a 69,XXX triploid premature infant
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Long-term survival in a 69,XXX triploid premature infant

American journal of medical genetics. Part A, 2008-06, Vol.146A (12), p.1618-1621 [Peer Reviewed Journal]

Copyright © 2008 Wiley‐Liss, Inc. ;2008 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.32352 ;PMID: 18478596

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13
Management of Pregnancy Achieved by Oocyte Donation to a Woman with 47,XXX and POF
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Management of Pregnancy Achieved by Oocyte Donation to a Woman with 47,XXX and POF

Journal of Mammalian Ova Research, 2011-10, Vol.28 (3), p.139-143

ISSN: 1341-7738

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14
A case of full triploidy (69,XXX) of paternal origin with unusually long survival time
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A case of full triploidy (69,XXX) of paternal origin with unusually long survival time

Clinical genetics, 1993-02, Vol.43 (2), p.79-82 [Peer Reviewed Journal]

1993 Blackwell Munksgaard ;1993 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1993.tb04432.x ;PMID: 8448906 ;CODEN: CLGNAY

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15
Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature
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Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature

Fetal diagnosis and therapy, 2010-03, Vol.27 (2), p.113-117 [Peer Reviewed Journal]

2010 S. Karger AG, Basel ;2015 INIST-CNRS ;2010 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426

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16
Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing
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Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing

Clinical chemistry (Baltimore, Md.), 2014-01, Vol.60 (1), p.251-259 [Peer Reviewed Journal]

COPYRIGHT 2014 American Association for Clinical Chemistry, Inc. ;Copyright American Association for Clinical Chemistry Jan 2014 ;ISSN: 0009-9147 ;EISSN: 1530-8561 ;DOI: 10.1373/clinchem.2013.215145 ;PMID: 24193117

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17
First report of a patient with a mixoploidy 47,XXX/94,XXXXXX
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First report of a patient with a mixoploidy 47,XXX/94,XXXXXX

Genetic counseling, 2007, Vol.18 (1), p.99-104 [Peer Reviewed Journal]

Copyright Editions Medecine et Hygiene 2007 ;ISSN: 1015-8146 ;PMID: 17515305

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18
Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China
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Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China

Journal of assisted reproduction and genetics, 2021-03, Vol.38 (3), p.727-734 [Peer Reviewed Journal]

The Author(s) 2021 ;The Author(s) 2021. 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: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-020-02056-2 ;PMID: 33564935

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19
Counting‐based cell‐free DNA screening test fails to identify triploidy—A case report
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Counting‐based cell‐free DNA screening test fails to identify triploidy—A case report

Clinical case reports, 2019-01, Vol.7 (1), p.90-93 [Peer Reviewed Journal]

2018 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/ccr3.1812 ;PMID: 30656016

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20
The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China
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The correlation between maternal age and fetal sex chromosome aneuploidies: a 8-year single institution experience in China

Molecular cytogenetics, 2021-05, Vol.14 (1), p.25-25, Article 25 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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) 2021 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-021-00545-2 ;PMID: 33971935

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