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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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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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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 |
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47,XXX male: A clinical and molecular studyAmerican journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Peer Reviewed Journal]Copyright © 2001 Wiley‐Liss, Inc. ;2001 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/1096-8628(20010201)98:4<353::AID-AJMG1110>3.0.CO;2-D ;PMID: 11170081 ;CODEN: AJMGDAFull text available |
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Malignant stromal tumour of the ovary with virilizing effects in an XXX female with streak ovaries. Clinical and pathological studiesAustralian & New Zealand journal of obstetrics & gynaecology, 1980-05, Vol.20 (2), p.123-128 [Peer Reviewed Journal]ISSN: 0004-8666 ;EISSN: 1479-828X ;DOI: 10.1111/j.1479-828X.1980.tb00110.x ;PMID: 6932203Full text available |
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Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospitalUltrasound in obstetrics & gynecology, 2014-07, Vol.44 (1), p.17 [Peer Reviewed Journal]Copyright © 2014 ISUOG. Published by John Wiley & Sons Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.13361 ;PMID: 24616044Digital Resources/Online E-Resources |
| 6 |
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Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in IranFetal diagnosis and therapy, 2020-03, Vol.47 (3), p.220-227 [Peer Reviewed Journal]2019 S. Karger AG, Basel ;2019 S. Karger AG, Basel. ;COPYRIGHT 2020 S. Karger AG ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000501014 ;PMID: 31487708Digital Resources/Online E-Resources |
| 7 |
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Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencingObstetrics and gynecology (New York. 1953), 2012-05, Vol.119 (5), p.890 [Peer Reviewed Journal]EISSN: 1873-233X ;DOI: 10.1097/AOG.0b013e31824fb482 ;PMID: 22362253Digital Resources/Online E-Resources |
| 8 |
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Screening for Sex Chromosome Aneuploidy by Cell-Free DNA Testing: Patient Choice and PerformanceFetal diagnosis and therapy, 2018-01, Vol.44 (2), p.98-104 [Peer Reviewed Journal]2017 S. Karger AG, Basel ;2017 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000479507 ;PMID: 28848190Digital Resources/Online E-Resources |
| 9 |
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Psychosocial Predictors of BRCA Counseling and Testing Decisions among Urban African-American WomenCancer epidemiology, biomarkers & prevention, 2002-12, Vol.11 (12), p.1579-1585 [Peer Reviewed Journal]2003 INIST-CNRS ;ISSN: 1055-9965 ;EISSN: 1538-7755 ;PMID: 12496047Full text available |
| 10 |
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Hysteroscopic management of a stenotic cervixFertility and sterility, 2017-06, Vol.107 (6), p.e19-e19 [Peer Reviewed Journal]American Society for Reproductive Medicine ;2017 American Society for Reproductive Medicine ;Copyright © 2017 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved. ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2017.03.027 ;PMID: 28577618Full text available |
| 11 |
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Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culturePrenatal diagnosis, 2003-10, Vol.23 (10), p.847-850 [Peer Reviewed Journal]Copyright © 2003 John Wiley & Sons, Ltd. ;2004 INIST-CNRS ;Copyright 2003 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.706 ;PMID: 14558031 ;CODEN: PRDIDMFull text available |
| 12 |
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Ear and hearing problems in 44 middle-aged women with Turner's syndromeHearing research, 1994-06, Vol.76 (1), p.127-132 [Peer Reviewed Journal]1994 ;1994 INIST-CNRS ;ISSN: 0378-5955 ;EISSN: 1878-5891 ;DOI: 10.1016/0378-5955(94)90094-9 ;PMID: 7928705 ;CODEN: HERED3Full text available |
| 13 |
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Chromosomal abnormalities in couples with history of recurrent abortionRevista Brasileira de ginecologia e obstetrícia, 2009-02, Vol.31 (2), p.68-74 [Peer Reviewed Journal]EISSN: 1806-9339 ;DOI: 10.1590/S0100-72032009000200004 ;PMID: 19407911Full text available |
| 14 |
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Testicular seminoma metastasizing to the parotid gland: Report of a caseHead & neck, 2005-10, Vol.27 (10), p.923-926 [Peer Reviewed Journal]Copyright © 2005 Wiley Periodicals, Inc. ;2005 INIST-CNRS ;(c) 2005 Wiley Periodicals, Inc. ;ISSN: 1043-3074 ;EISSN: 1097-0347 ;DOI: 10.1002/hed.20229 ;PMID: 15920749Full text available |
| 15 |
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Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocentesesPrenatal diagnosis, 1984-11, Vol.4 (7), p.5-44 [Peer Reviewed Journal]Copyright © 1984 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970040704 ;PMID: 6235485Full text available |
| 16 |
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Maternal serum Schwangerschafts protein-1 (SP1) and fetal chromosomal abnormalities at 10–13 weeks' gestationEarly human development, 1995-08, Vol.43 (1), p.31-36 [Peer Reviewed Journal]1995 ;1995 INIST-CNRS ;ISSN: 0378-3782 ;EISSN: 1872-6232 ;DOI: 10.1016/0378-3782(95)01658-P ;PMID: 8575349 ;CODEN: EHDEDNFull text available |
| 17 |
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ESTABLISHMENT AND APPLICATION OF A NORMAL RANGE FOR NUCHAL TRANSLUCENCY ACROSS THE FIRST TRIMESTERPrenatal diagnosis, 1996-07, Vol.16 (7), p.629-634 [Peer Reviewed Journal]Copyright © 1996 John Wiley & Sons, Ltd. ;1996 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/(SICI)1097-0223(199607)16:7<629::AID-PD922>3.0.CO;2-X ;PMID: 8843472 ;CODEN: PRDIDMFull text available |
| 18 |
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Genetics and biology of human ovarian teratomas. I, Cytogenetic analysis and mechanism of originAmerican journal of human genetics, 1990-10, Vol.47 (4), p.635-643 [Peer Reviewed Journal]1991 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 2220805 ;CODEN: AJHGAGFull text available |
| 19 |
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Sertoli–Leydig cell tumour complicated by X chromosomal mosaicismClinical endocrinology (Oxford), 1997-11, Vol.47 (5), p.619-622 [Peer Reviewed Journal]Blackwell Science Ltd, Oxford ;1998 INIST-CNRS ;ISSN: 0300-0664 ;EISSN: 1365-2265 ;DOI: 10.1046/j.1365-2265.1997.3031131.x ;PMID: 9425402 ;CODEN: CLECAPFull text available |
| 20 |
Material Type: Article
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Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndromeJournal of medical genetics, 1994-01, Vol.31 (1), p.76-78 [Peer Reviewed Journal]1994 INIST-CNRS ;Copyright BMJ Publishing Group LTD Jan 1994 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.31.1.76 ;PMID: 8151646 ;CODEN: JMDGAEFull text available |
Results 1 - 20 of 138 for All Library Resources
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