skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 259  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 5 next page
Refined by: Journal Title: Prenatal Diagnosis remove subject: Adult remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Rare autosomal trisomies: Important and not so rare
Rare autosomal trisomies: Important and not so rare
Material Type:
Article 		Add to My Research

Rare autosomal trisomies: Important and not so rare

Prenatal diagnosis, 2018-09, Vol.38 (10), p.765 [Peer Reviewed Journal]

2018 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5325 ;PMID: 29956348

Digital Resources/Online E-Resources

Citations Cited by
2
A systematic review of maternal TORCH serology as a screen for suspected fetal infection
A systematic review of maternal TORCH serology as a screen for suspected fetal infection
Material Type:
Article 		Add to My Research

A systematic review of maternal TORCH serology as a screen for suspected fetal infection

Prenatal diagnosis, 2022-01, Vol.42 (1), p.87 [Peer Reviewed Journal]

2021 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6073 ;PMID: 34893980

Digital Resources/Online E-Resources

Citations Cited by
3
Fetal phenotypes emerge as genetic technologies become robust
Fetal phenotypes emerge as genetic technologies become robust
Material Type:
Article 		Add to My Research

Fetal phenotypes emerge as genetic technologies become robust

Prenatal diagnosis, 2019-08, Vol.39 (9), p.811 [Peer Reviewed Journal]

2019 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5532 ;PMID: 31330568

Digital Resources/Online E-Resources

Citations Cited by
4
The clinical utility of genome-wide non invasive prenatal screening
The clinical utility of genome-wide non invasive prenatal screening
Material Type:
Article 		Add to My Research

The clinical utility of genome-wide non invasive prenatal screening

Prenatal diagnosis, 2017-06, Vol.37 (6), p.593 [Peer Reviewed Journal]

2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5053 ;PMID: 28423190

Digital Resources/Online E-Resources

Citations Cited by
5
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing
Material Type:
Article 		Add to My Research

Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing

Prenatal diagnosis, 2018-12, Vol.38 (13), p.1069 [Peer Reviewed Journal]

2018 The Authors Prenatal Diagnosis Published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5377 ;PMID: 30357877

Digital Resources/Online E-Resources

Citations Cited by
6
Non-invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods
Non-invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods
Material Type:
Article 		Add to My Research

Non-invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods

Prenatal diagnosis, 2021-10, Vol.41 (11), p.1395 [Peer Reviewed Journal]

2021 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6043 ;PMID: 34505288

Digital Resources/Online E-Resources

Citations Cited by
7
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes
Material Type:
Article 		Add to My Research

Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

Prenatal diagnosis, 2024-05, Vol.44 (5), p.586 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6554 ;PMID: 38558419

Digital Resources/Online E-Resources

Citations Cited by
8
Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype
Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype
Material Type:
Article 		Add to My Research

Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype

Prenatal diagnosis, 2024-05, Vol.44 (5), p.665 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6563 ;PMID: 38554254

Digital Resources/Online E-Resources

Citations Cited by
9
Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism
Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism
Material Type:
Article 		Add to My Research

Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism

Prenatal diagnosis, 2024-05, Vol.44 (5), p.562 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6558 ;PMID: 38520498

Digital Resources/Online E-Resources

Citations Cited by
10
"The anxiety coming up to every scan-It destroyed me": A qualitative study of the lived experience of cytomegalovirus infection during pregnancy
"The anxiety coming up to every scan-It destroyed me": A qualitative study of the lived experience of cytomegalovirus infection during pregnancy
Material Type:
Article 		Add to My Research

"The anxiety coming up to every scan-It destroyed me": A qualitative study of the lived experience of cytomegalovirus infection during pregnancy

Prenatal diagnosis, 2024-05, Vol.44 (5), p.623 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6564 ;PMID: 38578535

Digital Resources/Online E-Resources

Citations Cited by
11
Deep-learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy
Deep-learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy
Material Type:
Article 		Add to My Research

Deep-learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy

Prenatal diagnosis, 2024-05, Vol.44 (5), p.535 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6559 ;PMID: 38558081

Digital Resources/Online E-Resources

Citations Cited by
12
Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey
Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey
Material Type:
Article 		Add to My Research

Prenatal diagnosis (or lack thereof) of arthrogryposis multiplex congenita and its impact on the perinatal experience of parents: A retrospective survey

Prenatal diagnosis, 2024-05, Vol.44 (5), p.614 [Peer Reviewed Journal]

2024 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6569 ;PMID: 38578615

Digital Resources/Online E-Resources

Citations Cited by
13
Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus
Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus
Material Type:
Article 		Add to My Research

Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus

Prenatal diagnosis, 2024-05, Vol.44 (5), p.657 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6546 ;PMID: 38498110

Digital Resources/Online E-Resources

Citations Cited by
14
Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2
Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2
Material Type:
Article 		Add to My Research

Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2

Prenatal diagnosis, 2024-05, Vol.44 (5), p.661 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6560 ;PMID: 38549198

Digital Resources/Online E-Resources

Citations Cited by
15
Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk
Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk
Material Type:
Article 		Add to My Research

Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk

Prenatal diagnosis, 2024-05, Vol.44 (5), p.644 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6547 ;PMID: 38502037

Digital Resources/Online E-Resources

Citations Cited by
16
Postmortem imaging of fetuses at early gestations: A comparison of microfocus computed tomography with postmortem magnetic resonance at 9.4 T and postmortem ultrasound
Postmortem imaging of fetuses at early gestations: A comparison of microfocus computed tomography with postmortem magnetic resonance at 9.4 T and postmortem ultrasound
Material Type:
Article 		Add to My Research

Postmortem imaging of fetuses at early gestations: A comparison of microfocus computed tomography with postmortem magnetic resonance at 9.4 T and postmortem ultrasound

Prenatal diagnosis, 2024-05, Vol.44 (5), p.572 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6532 ;PMID: 38367004

Digital Resources/Online E-Resources

Citations Cited by
17
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene
Material Type:
Article 		Add to My Research

Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene

Prenatal diagnosis, 2024-02, Vol.44 (2), p.251 [Peer Reviewed Journal]

2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6501 ;PMID: 38141042

Digital Resources/Online E-Resources

Citations Cited by
18
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?
Material Type:
Article 		Add to My Research

Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?

Prenatal diagnosis, 2021-09, Vol.41 (10), p.1264 [Peer Reviewed Journal]

2021 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6031 ;PMID: 34405430

Digital Resources/Online E-Resources

Citations Cited by
19
The association between anticoagulation therapy, maternal characteristics, and a failed cfDNA test due to a low fetal fraction
The association between anticoagulation therapy, maternal characteristics, and a failed cfDNA test due to a low fetal fraction
Material Type:
Article 		Add to My Research

The association between anticoagulation therapy, maternal characteristics, and a failed cfDNA test due to a low fetal fraction

Prenatal diagnosis, 2017-11, Vol.37 (11), p.1125 [Peer Reviewed Journal]

2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5152 ;PMID: 28881030

Digital Resources/Online E-Resources

Citations Cited by
20
The near disappearance of fetal hydrops in relation to current state-of-the-art management of red cell alloimmunization
The near disappearance of fetal hydrops in relation to current state-of-the-art management of red cell alloimmunization
Material Type:
Article 		Add to My Research

The near disappearance of fetal hydrops in relation to current state-of-the-art management of red cell alloimmunization

Prenatal diagnosis, 2018-11, Vol.38 (12), p.943 [Peer Reviewed Journal]

2018 The Authors Prenatal Diagnosis Published by John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5355 ;PMID: 30187936

Digital Resources/Online E-Resources

Citations Cited by

Results 1 - 20 of 259  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Refine My Results

Creation Date 

From To
Refine
  1. Before 1994  (4)
  2. 1994 To 2008  (9)
  3. 2009 To 2013  (48)
  4. 2014 To 2018  (80)
  5. After 2018  (119)
  6. More options open sub menu
INSPIRE LIBRARY - TON DUC THANG UNIVERSITY (84-028) 37 755 057 Feedback
19 Nguyen Huu Tho St. Dist.7, HCM thuvien@tdtu.edu.vn

Copyright © 2017 INSPIRE LIBRARY - TON DUC THANG UNIVERSITY

Searching Remote Databases, Please Wait