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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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Prenatal diagnosis of 47,XXXAmerican journal of obstetrics and gynecology, 2005-05, Vol.192 (5), p.1469 [Peer Reviewed Journal]ISSN: 0002-9378 ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2004.12.037 ;PMID: 15902140Digital Resources/Online E-Resources |
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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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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 |
| 4 |
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Spontaneous pregnancy in a woman with 45,X/47,XXX mosaicism in both serum and germ cell lines. A case reportJournal of reproductive medicine, 2003-02, Vol.48 (2), p.121 [Peer Reviewed Journal]ISSN: 0024-7758 ;EISSN: 1943-3565 ;PMID: 12621797Digital Resources/Online E-Resources |
| 5 |
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21Journal of medical genetics, 1995-08, Vol.32 (8), p.650-653 [Peer Reviewed Journal]1995 INIST-CNRS ;Copyright BMJ Publishing Group LTD Aug 1995 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.32.8.650 ;PMID: 7473661 ;CODEN: JMDGAEFull text available |
| 6 |
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Prenatal diagnosis and prognosis of triple X syndrome: 47, XXXJournal de gynécologie, obstétrique et biologie de la reproduction, 2009-11, Vol.38 (7), p.599-6032009 Elsevier Masson SAS ;2009 INIST-CNRS ;ISSN: 0368-2315 ;DOI: 10.1016/j.jgyn.2009.08.003 ;PMID: 19762167 ;CODEN: JGOBACFull text available |
| 7 |
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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 |
| 8 |
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Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosisEuropean journal of pediatrics, 2010-10, Vol.169 (10), p.1255-1261 [Peer Reviewed Journal]Springer-Verlag 2010 ;2015 INIST-CNRS ;ISSN: 0340-6199 ;EISSN: 1432-1076 ;DOI: 10.1007/s00431-010-1221-8 ;PMID: 20473517 ;CODEN: EJPEDTFull text available |
| 9 |
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Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second TrimesterFetal 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: 10720874Full text available |
| 10 |
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Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorionPrenatal diagnosis, 1992-12, Vol.12 (12), p.1043-1046 [Peer Reviewed Journal]Copyright © 1992 John Wiley & Sons, Ltd. ;1993 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970121210 ;PMID: 1283786 ;CODEN: PRDIDMFull text available |
| 11 |
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Monozygotic Twinning in a Female with Triple X [47, XXX]Gynecologic and obstetric investigation, 1994, Vol.37 (4), p.279-280 [Peer Reviewed Journal]1994 S. Karger AG, Basel ;1994 INIST-CNRS ;ISSN: 0378-7346 ;EISSN: 1423-002X ;DOI: 10.1159/000292578 ;PMID: 8050736 ;CODEN: GOBIDSDigital Resources/Online E-Resources |
| 12 |
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Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalitiesAmerican journal of medical genetics, 2002-06, Vol.110 (1), p.11-18 [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.10394 ;PMID: 12116265 ;CODEN: AJMGDAFull text available |
| 13 |
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Triple X syndrome with rare phenotypic presentationIndian journal of pediatrics, 2008-06, Vol.75 (6), p.629-631 [Peer Reviewed Journal]Dr. K C Chaudhuri Foundation 2008 ;2008 INIST-CNRS ;ISSN: 0019-5456 ;EISSN: 0973-7693 ;DOI: 10.1007/s12098-008-0120-8 ;PMID: 18759093 ;CODEN: IJPEA2Full text available |
| 14 |
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Research on heterocyclic compounds. XXX. Synthesis and pharmacological activity of 2-methylimidazo[1,2-b]pyridazine-3-carboxylic acidsFarmaco (Società chimica italiana : 1989), 1992-06, Vol.47 (6), p.931 [Peer Reviewed Journal]ISSN: 0014-827X ;EISSN: 1879-0569 ;PMID: 1388610Digital Resources/Online E-Resources |
| 15 |
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 |
| 16 |
Material Type: Article
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A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXYHuman genetics, 1984-01, Vol.66 (4), p.367-369 [Peer Reviewed Journal]1985 INIST-CNRS ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00287644 ;PMID: 6586638 ;CODEN: HUGEDQFull text available |
| 17 |
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Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomiesAmerican journal of medical genetics, 1998-12, Vol.80 (4), p.330-334 [Peer Reviewed Journal]Copyright © 1998 Wiley‐Liss, Inc. ;1999 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/(SICI)1096-8628(19981204)80:4<330::AID-AJMG6>3.0.CO;2-7 ;PMID: 9856559 ;CODEN: AJMGDAFull text available |
| 18 |
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Evidence of a second gameter fusion after the first cleavage of the zygote in a 47,XX,+18/70,XXX,+18 mosaic. A remarkable diploid-triploid discrepancy after CVSPrenatal diagnosis, 1993, Vol.13 (4), p.301-306 [Peer Reviewed Journal]1993 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;CODEN: PRDIDMFull text available |
| 19 |
Material Type: Article
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Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetusAmerican journal of medical genetics, 1989-06, Vol.33 (2), p.242-243 [Peer Reviewed Journal]Copyright © 1989 Wiley‐Liss, Inc., A Wiley Company ;1989 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320330220 ;PMID: 2669483 ;CODEN: AJMGDAFull text available |
| 20 |
Material Type: Article
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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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