Results 1 - 20 of 218 for All Library Resources
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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 |
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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 |
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Different patterns of chromosomal imbalances in metastasising and non-metastasising primary breast carcinomasInternational journal of cancer, 1999-08, Vol.84 (4), p.370 [Peer Reviewed Journal]Copyright 1999 Wiley-Liss, Inc. ;ISSN: 0020-7136 ;EISSN: 1097-0215 ;DOI: 10.1002/(SICI)1097-0215(19990820)84:4<370::AID-IJC7>3.0.CO;2-7 ;PMID: 10404088Digital Resources/Online E-Resources |
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Evaluation of chromosomal abnormalities in the postnatal cohort: A single‐center study on 14,242 patientsJournal of clinical laboratory analysis, 2024-01, Vol.38 (1-2), p.e24997-n/a [Peer Reviewed Journal]2023 The Authors. published by Wiley Periodicals LLC. ;2023 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. ;2024. 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: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.24997 ;PMID: 38115218Full text available |
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Knowledge and attitude of pregnant women in the Kingdom of Saudi Arabia toward Noninvasive prenatal testing: A single center studyMolecular genetics & genomic medicine, 2022-07, Vol.10 (7), p.e1960-n/a [Peer Reviewed Journal]2022 The Authors. published by Wiley Periodicals LLC. ;2022 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1960 ;PMID: 35481946Full text available |
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Celebrating Baer ‐ a Nordic scientist who discovered the mammalian oocyteActa obstetricia et gynecologica Scandinavica, 2017-11, Vol.96 (11), p.1281-1282 [Peer Reviewed Journal]2017 Nordic Federation of Societies of Obstetrics and Gynecology ;Copyright © 2017 Acta Obstetricia et Gynecologica Scandinavica ;ISSN: 0001-6349 ;ISSN: 1600-0412 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.13234 ;PMID: 29034960Full text available |
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Association between different morphological types and abnormal karyotypes in early pregnancy lossUltrasound in obstetrics & gynecology, 2011-02, Vol.37 (2), p.219 [Peer Reviewed Journal]Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.7681 ;PMID: 20503243Digital Resources/Online E-Resources |
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Menstrual bleeding patterns in pre- and perimenopausal women: a population-based prospective diary studyActa obstetricia et gynecologica Scandinavica, 2004-02, Vol.83 (2), p.197-202 [Peer Reviewed Journal]2004 INIST-CNRS ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/j.0001-6349.2004.00401.x ;PMID: 14756740 ;CODEN: AOGSAEFull text available |
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Frequency of spontaneously occurring postmenopausal bleeding in the general populationActa obstetricia et gynecologica Scandinavica, 2004-02, Vol.83 (2), p.203-207 [Peer Reviewed Journal]2004 INIST-CNRS ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/j.0001-6349.2004.00400.x ;PMID: 14756741 ;CODEN: AOGSAEFull text available |
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A rapid and reliable chromosome analysis method for products of conception using interphase nucleiMolecular genetics & genomic medicine, 2018-05, Vol.6 (3), p.370-381 [Peer Reviewed Journal]2018 InteGen LLC. published by Wiley Periodicals, Inc. ;2018 InteGen LLC. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2018. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.381 ;PMID: 29573570Full text available |
| 11 |
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Non-invasive cell-free DNA-based approach for the diagnosis of clinical miscarriage: A retrospective studyBJOG : an international journal of obstetrics and gynaecology, 2024-01, Vol.131 (2), p.213 [Peer Reviewed Journal]2023 John Wiley & Sons Ltd. ;EISSN: 1471-0528 ;DOI: 10.1111/1471-0528.17629 ;PMID: 37533357Digital Resources/Online E-Resources |
| 12 |
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Provoked Vestibulodynia in Women with Pelvic PainSexual medicine, 2019-06, Vol.7 (2), p.227-234 [Peer Reviewed Journal]2019 The Authors ;Copyright © 2019. Published by Elsevier Inc. ;2019 The Authors 2019 ;ISSN: 2050-1161 ;EISSN: 2050-1161 ;DOI: 10.1016/j.esxm.2019.03.002 ;PMID: 30954496Full text available |
| 13 |
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Diagnosis and prediction of parental origin of triploidies by fetal nuchal translucency and maternal serum free -hCG and PAPP-A at 11-14 weeks of gestationActa obstetricia et gynecologica Scandinavica, 2008, Vol.87 (9), p.975-978 [Peer Reviewed Journal]2008 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2008 ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1080/00016340802275927Full text available |
| 14 |
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Diagnosis and prediction of parental origin of triploidies by fetal nuchal translucency and maternal serum free β-hCG and PAPP-A at 11-14 weeks of gestationActa obstetricia et gynecologica Scandinavica, 2008-01, Vol.87 (9), p.975-978 [Peer Reviewed Journal]Acta Obstet Gynecol Scand 2008 ;2008 INIST-CNRS ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1080/00016340802275927 ;PMID: 18720036 ;CODEN: AOGSAEFull text available |
| 15 |
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Allogeneic marrow grafts from donors with congenital chromosomal abnormalities in marrow cellsBritish journal of haematology, 1995-07, Vol.90 (3), p.595-601 [Peer Reviewed Journal]1995 INIST-CNRS ;ISSN: 0007-1048 ;EISSN: 1365-2141 ;DOI: 10.1111/j.1365-2141.1995.tb05589.x ;PMID: 7646999 ;CODEN: BJHEALFull text available |
| 16 |
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Fetal gender and sonographic assessment of crown-rump length: implications for multifetal pregnancy reductionUltrasound in obstetrics & gynecology, 2004-09, Vol.24 (4), p.399 [Peer Reviewed Journal]Copyright 2004 ISUOG ;ISSN: 0960-7692 ;EISSN: 1469-0705 ;DOI: 10.1002/uog.1084 ;PMID: 15343593Digital Resources/Online E-Resources |
| 17 |
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Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variantsPrenatal diagnosis, 2023-02, Vol.43 (2), p.192 [Peer Reviewed Journal]2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6320 ;PMID: 36726284Digital Resources/Online E-Resources |
| 18 |
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Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcomePrenatal diagnosis, 2023-02, Vol.43 (2), p.183 [Peer Reviewed Journal]2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6302 ;PMID: 36600414Digital Resources/Online E-Resources |
| 19 |
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Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyPrenatal diagnosis, 2024-03, Vol.44 (3), p.304 [Peer Reviewed Journal]2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6529 ;PMID: 38411249Digital Resources/Online E-Resources |
| 20 |
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Huge acoustic neurinomas presenting in the late stage of pregnancyActa obstetricia et gynecologica Scandinavica, 2001-02, Vol.80 (2), p.179-184 [Peer Reviewed Journal]ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1034/j.1600-0412.2001.080002179.xFull text available |
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