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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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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort studyOrphanet 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: 30642344Full text available |
| 2 |
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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 |
| 3 |
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Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XXThe 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: 23937348Full text available |
| 4 |
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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 |
| 5 |
Material Type: Article
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Long-term survival in a 69,XXX triploid premature infantAmerican 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: 18478596Full text available |
| 6 |
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 |
| 7 |
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 |
| 8 |
Material Type: Article
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Long survival in a 69,XXX triploid infant in GreeceGenetics and molecular research, 2005-12, Vol.4 (4), p.755-759 [Peer Reviewed Journal]ISSN: 1676-5680 ;EISSN: 1676-5680 ;PMID: 16475122Full text available |
| 9 |
Material Type: Article
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, IndiaJournal of genetics, 2008-12, Vol.87 (3), p.257-259 [Peer Reviewed Journal]Indian Academy of Sciences 2008 ;ISSN: 0022-1333 ;EISSN: 0973-7731 ;DOI: 10.1007/s12041-008-0039-x ;PMID: 19147910Full text available |
| 10 |
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 |
| 11 |
Material Type: Article
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Trisomy 8 mosaicism in a patient born to a mother with 47,XXXAmerican journal of medical genetics. Part A, 2003-05, Vol.119A (1), p.85-86 [Peer Reviewed Journal]Copyright © 2003 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20086 ;PMID: 12707966Full text available |
| 12 |
Material Type: Article
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Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidyJournal of medical genetics, 1993-07, Vol.30 (7), p.597-600 [Peer Reviewed Journal]1993 INIST-CNRS ;Copyright BMJ Publishing Group LTD Jul 1993 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.30.7.597 ;PMID: 8411035 ;CODEN: JMDGAEFull text available |
| 13 |
Material Type: Article
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Double trisomy (48,XXX, + 18)American journal of medical genetics, 1994-08, Vol.52 (2), p.244-244 [Peer Reviewed Journal]Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320520227 ;PMID: 7802021Full text available |
| 14 |
Material Type: Article
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46,XX/69,XXX diploid-triploid mixoploidy with hypothyroidism and precocious pubertyJournal of medical genetics, 1993-11, Vol.30 (11), p.966-967 [Peer Reviewed Journal]1994 INIST-CNRS ;Copyright BMJ Publishing Group LTD Nov 1993 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.30.11.966 ;PMID: 8301657 ;CODEN: JMDGAEFull text available |
| 15 |
Material Type: Article
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An infant with double trisomy (48,XXX, + 18)American journal of medical genetics, 1994-01, Vol.49 (2), p.207-210 [Peer Reviewed Journal]Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company ;1994 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320490210 ;PMID: 8116670 ;CODEN: AJMGDAFull text available |
| 16 |
Material Type: Article
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Multiple congenital anomalies associated with a 47,XXX chromosome constitutionAmerican journal of medical genetics, 1990-05, Vol.36 (1), p.73-75 [Peer Reviewed Journal]Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320360114 ;PMID: 2333909Full text available |
| 17 |
Material Type: Article
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47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformationAmerican journal of medical genetics, 1988-03, Vol.29 (3), p.511-515 [Peer Reviewed Journal]Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company ;1989 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320290306 ;PMID: 3376994 ;CODEN: AJMGDAFull text available |
| 18 |
Material Type: Article
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A case of liveborn triploidy (69,XXX)Acta pædiatrica Scandinavica, 1972-03, Vol.61 (2), p.203-208 [Peer Reviewed Journal]ISSN: 0001-656X ;DOI: 10.1111/j.1651-2227.1972.tb15925.x ;PMID: 4622018Full text available |
| 19 |
Material Type: Article
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Lymphocyte proliferation in a 31-week premature neonate with 69, XXX chromosomal constitutionClinical genetics, 1983-07, Vol.24 (1), p.26-28 [Peer Reviewed Journal]ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1983.tb00064.x ;PMID: 6616943Full text available |
| 20 |
Material Type: Article
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Diplospermy II indicated as the origin of a liveborn human triploid (69,XXX)Journal of medical genetics, 1981-10, Vol.18 (5), p.386-389 [Peer Reviewed Journal]Copyright BMJ Publishing Group LTD Oct 1981 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.18.5.386 ;PMID: 6948962 ;CODEN: JMDGAEFull text available |
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