Results 1 - 20 of 1,014 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Article
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Mortality and incidence in women with 47,XXX and variantsAmerican journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Peer Reviewed Journal]Copyright © 2010 Wiley‐Liss, Inc. ;Copyright 2010 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.33214 ;PMID: 20101696Full text available |
| 2 |
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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 |
| 3 |
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Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful kneeClinical and experimental rheumatology, 2010-11, Vol.28 (6), p.803-805 [Peer Reviewed Journal]2015 INIST-CNRS ;ISSN: 0392-856X ;EISSN: 1593-098X ;PMID: 21205458Full text available |
| 4 |
Material Type: Article
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular eventsRheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Peer Reviewed Journal]2005 INIST-CNRS ;Copyright Oxford University Press(England) Jul 2005 ;ISSN: 1462-0324 ;EISSN: 1462-0332 ;DOI: 10.1093/rheumatology/keh613 ;PMID: 15797975 ;CODEN: BJRHDFFull text available |
| 5 |
Material Type: Article
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47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal developmentFertility and sterility, 2009-11, Vol.92 (5), p.1747.e5-1747.e7 [Peer Reviewed Journal]American Society for Reproductive Medicine ;2009 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2009.07.1008 ;PMID: 19732877Full text available |
| 6 |
Material Type: Article
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The craniofacial complex in 47, XXX femalesEuropean journal of orthodontics, 2005-08, Vol.27 (4), p.396-401 [Peer Reviewed Journal]ISSN: 0141-5387 ;EISSN: 1460-2210 ;DOI: 10.1093/ejo/cji016 ;PMID: 16043476 ;CODEN: EJOODKFull text available |
| 7 |
Material Type: Article
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypesAmerican journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Peer Reviewed Journal]Copyright © 2001 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.10154 ;PMID: 11840512 ;CODEN: AJMGDAFull text available |
| 8 |
Material Type: Article
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Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXXBirth defects research. A Clinical and molecular teratology, 2007-08, Vol.79 (8), p.612-613 [Peer Reviewed Journal]Copyright © 2007 Wiley‐Liss, Inc. ;2007 Wiley-Liss, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.20371 ;PMID: 17469201Full text available |
| 9 |
Material Type: Article
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Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX MosaicismInternal Medicine, 2009, Vol.48(6), pp.447-453 [Peer Reviewed Journal]2009 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.48.1157 ;PMID: 19293545Full text available |
| 10 |
Material Type: Article
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Kallmann syndrome in a 47,XXX patientAmerican journal of medical genetics. Part A, 2005-11, Vol.139A (1), p.52-53 [Peer Reviewed Journal]Copyright © 2005 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.30996 ;PMID: 16222664Full text available |
| 11 |
Material Type: Article
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two casesPrenatal 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: 15614873Full text available |
| 12 |
Material Type: Article
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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 LiteratureFetal 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: 20160426Full text available |
| 13 |
Material Type: Article
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A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotypeEndokrynologia polska, 2010-03, Vol.61 (2), p.217-219 [Peer Reviewed Journal]2010. 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: 0423-104X ;PMID: 20464710Full text available |
| 14 |
Material Type: Article
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Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXXJournal of the American Academy of Child and Adolescent Psychiatry, 1998-03, Vol.37 (3), p.286-291 [Peer Reviewed Journal]1998 The American Academy of Child and Adolescent Psychiatry ;1998 INIST-CNRS ;Copyright Lippincott Williams & Wilkins Mar 1998 ;ISSN: 0890-8567 ;EISSN: 1527-5418 ;DOI: 10.1097/00004583-199803000-00013 ;PMID: 9519633 ;CODEN: JAAPEEFull text available |
| 15 |
Material Type: Article
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Female-to-male transsexual with 47,XXX karyotypeBiological psychiatry (1969), 2000-12, Vol.48 (11), p.1116-1117 [Peer Reviewed Journal]2000 Society of Biological Psychiatry ;2001 INIST-CNRS ;ISSN: 0006-3223 ;EISSN: 1873-2402 ;DOI: 10.1016/S0006-3223(00)00954-9 ;PMID: 11094147 ;CODEN: BIPCBFFull text available |
| 16 |
Material Type: Article
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Pituitary tumor in a woman with a 47,XXX karyotype--case reportMedical science monitor, 2001-03, Vol.7 (2), p.304-307ISSN: 1234-1010 ;EISSN: 1643-3750 ;PMID: 11257740Full text available |
| 17 |
Material Type: Article
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Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at pubertyThe Journal of pediatrics, 2001-11, Vol.139 (5), p.724-728 [Peer Reviewed Journal]2001 Mosby, Inc. ;2002 INIST-CNRS ;ISSN: 0022-3476 ;EISSN: 1097-6833 ;DOI: 10.1067/mpd.2001.118571 ;PMID: 11713453 ;CODEN: JOPDABFull text available |
| 18 |
Material Type: Article
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Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40‐year‐old woman with a mosaic Turner's karyotype (45,X/47,XXX)Acta obstetricia et gynecologica Scandinavica, 2003-08, Vol.82 (8), p.773-774 [Peer Reviewed Journal]ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1034/j.1600-0412.2003.00071.x ;PMID: 12848653Full text available |
| 19 |
Material Type: Article
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Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXXChromosome research, 2004-01, Vol.12 (2), p.125-132 [Peer Reviewed Journal]Kluwer Academic Publishers 2004. ;ISSN: 0967-3849 ;EISSN: 1573-6849 ;DOI: 10.1023/B:CHRO.0000013164.56757.bd ;PMID: 15053482Full text available |
| 20 |
Material Type: Article
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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]Copyright © 2000 John Wiley & Sons, Ltd. ;Copyright 2000 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E ;PMID: 11015706Full text available |
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