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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndromeJournal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Peer Reviewed Journal]Copyright 2002 Journal of Medical Genetics ;2002 INIST-CNRS ;COPYRIGHT 2002 BMJ Publishing Group Ltd. ;Copyright: 2002 Copyright 2002 Journal of Medical Genetics ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.39.3.217 ;PMID: 11897829 ;CODEN: JMDGAEFull text available |
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Peer Reviewed Journal]2000 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E ;CODEN: PRDIDMFull text available |
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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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XXX. Ueber das metastatische Ovarialcarcinom nach Krebs des Magens, Darmes und anderer Bauchorgane (Part 1 of 2)Gynecologic and obstetric investigation, 1902, Vol.15 (4), p.485-506 [Peer Reviewed Journal]1902 S. Karger AG, Basel ;ISSN: 0378-7346 ;EISSN: 1423-002X ;DOI: 10.1159/000283419Digital Resources/Online E-Resources |
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Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasmaPrenatal diagnosis, 2013-06, Vol.33 (6), p.591-597 [Peer Reviewed Journal]2013 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4127 ;PMID: 23592550Full text available |
| 6 |
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Variation in the decision to terminate pregnancy in the setting of fetal aneuploidyPrenatal diagnosis, 2006-08, Vol.26 (8), p.667-671 [Peer Reviewed Journal]Copyright © 2006 John Wiley & Sons, Ltd. ;2006 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1462 ;PMID: 16724363 ;CODEN: PRDIDMFull text available |
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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNAAmerican journal of obstetrics and gynecology, 2014-10, Vol.211 (4), p.365.e1 [Peer Reviewed Journal]Copyright © 2014 Elsevier Inc. All rights reserved. ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2014.03.042 ;PMID: 24657131Digital Resources/Online E-Resources |
| 8 |
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Is the prevalence of Klinefelter syndrome increasing?European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.163-170 [Peer Reviewed Journal]2008 INIST-CNRS ;Copyright Nature Publishing Group Feb 2008 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201956 ;PMID: 18000523Full text available |
| 9 |
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Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidyObstetrics and gynecology (New York. 1953), 2004-07, Vol.104 (1), p.94 [Peer Reviewed Journal]ISSN: 0029-7844 ;EISSN: 1873-233X ;DOI: 10.1097/01.aog.0000128171.14081.eb ;PMID: 15229006Digital Resources/Online E-Resources |
| 10 |
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Usefulness of combined NGS and QF‐PCR analysis for product of conception karyotypingReproductive medicine and biology, 2022-01, Vol.21 (1), p.e12449-n/a [Peer Reviewed Journal]2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. ;2022 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. ;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: 1445-5781 ;EISSN: 1447-0578 ;DOI: 10.1002/rmb2.12449 ;PMID: 35386384Full text available |
| 11 |
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Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndromePrenatal diagnosis, 2010-11, Vol.30 (11), p.1072-1078 [Peer Reviewed Journal]Copyright © 2010 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2613 ;PMID: 20842625 ;CODEN: PRDIDMFull text available |
| 12 |
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Assessing the role of placental trisomy in preeclampsia and intrauterine growth restrictionPrenatal diagnosis, 2010-01, Vol.30 (1), p.1-8 [Peer Reviewed Journal]Copyright © 2009 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;Copyright (c) 2009 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;ISSN: 1097-0223 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2409 ;PMID: 19918961 ;CODEN: PRDIDMFull text available |
| 13 |
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Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortionHuman reproduction update, 2000-01, Vol.6 (1), p.93-105 [Peer Reviewed Journal]ISSN: 1355-4786 ;EISSN: 1460-2369 ;DOI: 10.1093/humupd/6.1.93 ;PMID: 10711834 ;CODEN: HRUPF8Full text available |
| 14 |
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Parental decisions following the prenatal diagnosis of sex chromosome abnormalitiesEuropean journal of obstetrics & gynecology and reproductive biology, 2004-09, Vol.116 (1), p.58 [Peer Reviewed Journal]ISSN: 0301-2115 ;EISSN: 1872-7654 ;DOI: 10.1016/j.ejogrb.2003.12.029 ;PMID: 15294369Digital Resources/Online E-Resources |
| 15 |
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Crown-rump length in chromosomally abnormal fetuses at 10 to 13 weeks' gestationAmerican journal of obstetrics and gynecology, 1995, Vol.172 (1), p.32-35 [Peer Reviewed Journal]1995 ;1995 INIST-CNRS ;ISSN: 0002-9378 ;EISSN: 1097-6868 ;DOI: 10.1016/0002-9378(95)90080-2 ;PMID: 7847557 ;CODEN: AJOGAHFull text available |
| 16 |
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Pre-eclampsia and peripartum cardiomyopathy in molar pregnancy: clinical implication for maternally imprinted genesUltrasound in obstetrics & gynecology, 2004-04, Vol.23 (4), p.398 [Peer Reviewed Journal]Copyright 2004 ISUOG. ;ISSN: 0960-7692 ;EISSN: 1469-0705 ;DOI: 10.1002/uog.1015 ;PMID: 15065193Digital Resources/Online E-Resources |
| 17 |
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Pregnancy outcome and prenatal diagnosis of sex chromosome abnormalities in Hawaii, 1986-1999American journal of medical genetics. Part A, 2003-06, Vol.119A (3), p.305-310 [Peer Reviewed Journal]Copyright © 2003 Wiley‐Liss, Inc. ;Copyright 2003 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20150 ;PMID: 12784298Full text available |
| 18 |
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Cytogenetic results from the U.S. collaborative study on CVSPrenatal diagnosis, 1992-05, Vol.12 (5), p.317-345 [Peer Reviewed Journal]Copyright © 1992 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970120503 ;PMID: 1523201Full text available |
| 19 |
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Fluorescence in-situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46,XY/47,XXY maleHuman reproduction (Oxford), 2000-02, Vol.15 (2), p.440-444 [Peer Reviewed Journal]European Society of Human Reproduction and Embryology 2000 ;2000 INIST-CNRS ;ISSN: 0268-1161 ;ISSN: 1460-2350 ;EISSN: 1460-2350 ;DOI: 10.1093/humrep/15.2.440 ;PMID: 10655319 ;CODEN: HUREEEFull text available |
| 20 |
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Mosaic Turner syndrome: cytogenetics versus FISHAnnals of human genetics, 1999-05, Vol.63 (3), p.199-206 [Peer Reviewed Journal]University College London 1999 ;1999 University College London ;1999 INIST-CNRS ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1046/j.1469-1809.1999.6330199.x ;PMID: 10738532 ;CODEN: ANHGAAFull text available |
Results 1 - 20 of 127 for All Library Resources
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