skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index
Refined by: Database: MEDLINE remove subject: Ultrasonic Imaging remove xxx: xxx remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Prenatal and neonatal testing
Material Type:
Article
Add to My Research

Prenatal and neonatal testing

Clinical chemistry and laboratory medicine, 2023-05, Vol.61 (s1), p.s1961 [Peer Reviewed Journal]

EISSN: 1437-4331 ;DOI: 10.1515/cclm-2023-7060 ;PMID: 37037572

Digital Resources/Online E-Resources

2
Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities
Material Type:
Article
Add to My Research

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.725-730 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2013 ;Copyright © 2013 Macmillan Publishers Limited 2013 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2012.253 ;PMID: 23211699

Full text available

3
Clinical spectrum of female genital malformations in prenatal diagnosis
Material Type:
Article
Add to My Research

Clinical spectrum of female genital malformations in prenatal diagnosis

Archives of gynecology and obstetrics, 2022-12, Vol.306 (6), p.1847-1862 [Peer Reviewed Journal]

The Author(s) 2022 ;2022. The Author(s). ;The Author(s) 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: 1432-0711 ;ISSN: 0932-0067 ;EISSN: 1432-0711 ;DOI: 10.1007/s00404-022-06441-3 ;PMID: 35220478

Full text available

4
Combined diagnosis of QF‐PCR and CNV‐Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosis
Material Type:
Article
Add to My Research

Combined diagnosis of QF‐PCR and CNV‐Seq in fetal chromosomal abnormalities: A new perspective on prenatal diagnosis

Journal of clinical laboratory analysis, 2022-04, Vol.36 (4), p.e24311-n/a [Peer Reviewed Journal]

2022 The Authors. published by Wiley Periodicals LLC ;2022 The Authors. Journal of Clinical Laboratory Analysis 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: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.24311 ;PMID: 35195919

Full text available

5
Diagnosis and Management of Fetal and Neonatal Thyrotoxicosis
Material Type:
Article
Add to My Research

Diagnosis and Management of Fetal and Neonatal Thyrotoxicosis

Medicina (Kaunas, Lithuania), 2023-01, Vol.59 (1), p.36 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1648-9144 ;ISSN: 1010-660X ;EISSN: 1648-9144 ;DOI: 10.3390/medicina59010036 ;PMID: 36676660

Full text available

6
Use of tissue samples in diagnosing diploid triploid mosaicism
Material Type:
Article
Add to My Research

Use of tissue samples in diagnosing diploid triploid mosaicism

BMJ case reports, 2022-12, Vol.15 (12), p.e252779 [Peer Reviewed Journal]

BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;EISSN: 1757-790X ;DOI: 10.1136/bcr-2022-252779 ;PMID: 36593622

Full text available

7
Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli’s disease)
Material Type:
Article
Add to My Research

Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli’s disease)

Gut, 1999-11, Vol.45 (5), p.780-782 [Peer Reviewed Journal]

British Society of Gastroenterology ;1999 INIST-CNRS ;Copyright: 1999 British Society of Gastroenterology ;ISSN: 0017-5749 ;ISSN: 1468-3288 ;EISSN: 1468-3288 ;DOI: 10.1136/gut.45.5.780 ;PMID: 10517920 ;CODEN: GUTTAK

Full text available

Searching Remote Databases, Please Wait