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 385  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: Database: PubMed Central remove xxx: xxx remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
Material Type:
Article 		Add to My Research

A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/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/mgg3.1279 ;PMID: 32463164

Full text available

Citations Cited by
2
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
Material Type:
Article 		Add to My Research

Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome

Journal 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: JMDGAE

Full text available

Citations Cited by
3
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)
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)
Material Type:
Article 		Add to My Research

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: 12848653

Full text available

Citations Cited by
4
Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy
Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy
Material Type:
Article 		Add to My Research

Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy

Medicinski arhiv, 2017-04, Vol.71 (2), p.144-147 [Peer Reviewed Journal]

Copyright Academy of Medical Sciences of Bosnia and Herzegovina 2017 ;Copyright: © 2017 Milenko Kolarski, Begzudin Ahmetovic, Maja Beres, Radomir Topic, Vedran Nikic, Ivana Kavecan, Semin Sabic 2017 ;ISSN: 0350-199X ;EISSN: 1986-5961 ;DOI: 10.5455/medarh.2017.71.144-147 ;PMID: 28790549

Full text available

Citations Cited by
5
Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
Material Type:
Article 		Add to My Research

Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21

Journal 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: JMDGAE

Full text available

Citations Cited by
6
Fertility in 47,XXX and 45,X patients
Fertility in 47,XXX and 45,X patients
Material Type:
Article 		Add to My Research

Fertility in 47,XXX and 45,X patients

Journal of medical genetics, 1978-04, Vol.15 (2), p.132-135 [Peer Reviewed Journal]

Copyright BMJ Publishing Group LTD Apr 1978 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.15.2.132 ;PMID: 641947 ;CODEN: JMDGAE

Full text available

Citations Cited by
7
Prenatal diagnosis and gonadal findings in X/XXX mosaicism
Prenatal diagnosis and gonadal findings in X/XXX mosaicism
Material Type:
Article 		Add to My Research

Prenatal diagnosis and gonadal findings in X/XXX mosaicism

Journal of medical genetics, 1977-04, Vol.14 (2), p.120-123 [Peer Reviewed Journal]

Copyright BMJ Publishing Group LTD Apr 1977 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.14.2.120 ;PMID: 856232 ;CODEN: JMDGAE

Full text available

Citations Cited by
8
Antenatal diagnosis of an XXX female. A dilemma for genetic counseling
Antenatal diagnosis of an XXX female. A dilemma for genetic counseling
Material Type:
Article 		Add to My Research

Antenatal diagnosis of an XXX female. A dilemma for genetic counseling

The Western journal of medicine, 1975-07, Vol.123 (1), p.17-21 [Peer Reviewed Journal]

ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778

Full text available

Citations Cited by
9
Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1
Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1
Material Type:
Article 		Add to My Research

Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1

American journal of human genetics, 1981-07, Vol.33 (4), p.649-650 [Peer Reviewed Journal]

ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 7258190

Full text available

Citations Cited by
10
Prenatal diagnosis of triploidy (69, XXX) (author's transl)
Prenatal diagnosis of triploidy (69, XXX) (author's transl)
Material Type:
Article 		Add to My Research

Prenatal diagnosis of triploidy (69, XXX) (author's transl)

Geburtshilfe und Frauenheilkunde, 1979-07, Vol.39 (7), p.588-592 [Peer Reviewed Journal]

ISSN: 0016-5751 ;PMID: 467953

Digital Resources/Online E-Resources

Citations Cited by
11
Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man
Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man
Material Type:
Article 		Add to My Research

Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man

Journal of medical genetics, 1976-10, Vol.13 (5), p.371-380 [Peer Reviewed Journal]

Copyright BMJ Publishing Group LTD Oct 1976 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.13.5.371 ;PMID: 1034015 ;CODEN: JMDGAE

Full text available

Citations Cited by
12
Prenatal cytogenetic diagnosis of a 69,XXX/46,XX fetus
Prenatal cytogenetic diagnosis of a 69,XXX/46,XX fetus
Material Type:
Article 		Add to My Research

Prenatal cytogenetic diagnosis of a 69,XXX/46,XX fetus

Pathologica, 1985-11, Vol.77 (1052), p.761-766 [Peer Reviewed Journal]

ISSN: 0031-2983 ;EISSN: 1591-951X ;PMID: 3842997

Digital Resources/Online E-Resources

Citations Cited by
13
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases
Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases
Material Type:
Article 		Add to My Research

Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases

Molecular cytogenetics, 2021-01, Vol.14 (1), p.1-1, Article 1 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed 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. ;The Author(s) 2021 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-020-00521-2 ;PMID: 33407708

Full text available

Citations Cited by
14
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
Material Type:
Article 		Add to My Research

Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

PloS one, 2016-08, Vol.11 (8), p.e0161045-e0161045 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Samango-Sprouse et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Samango-Sprouse et al 2016 Samango-Sprouse et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0161045 ;PMID: 27512996

Full text available

Citations Cited by
15
Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report
Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report
Material Type:
Article 		Add to My Research

Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report

Medicine (Baltimore), 2020-07, Vol.99 (29), p.e20848-e20848 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020848 ;PMID: 32702826

Full text available

Citations Cited by
16
The Effect of Using Dexamethasone Tablets Vaginally for Improving Cervical Bishop Score in Nulliparous Pregnant Women: A Randomized Clinical Trial
The Effect of Using Dexamethasone Tablets Vaginally for Improving Cervical Bishop Score in Nulliparous Pregnant Women: A Randomized Clinical Trial
Material Type:
Article 		Add to My Research

The Effect of Using Dexamethasone Tablets Vaginally for Improving Cervical Bishop Score in Nulliparous Pregnant Women: A Randomized Clinical Trial

Current therapeutic research, 2023-01, Vol.98, p.100702-100702, Article 100702 [Peer Reviewed Journal]

2023 The Author(s) ;2023 The Author(s). ;2023 The Author(s) 2023 ;ISSN: 0011-393X ;EISSN: 1879-0313 ;DOI: 10.1016/j.curtheres.2023.100702 ;PMID: 37101983

Full text available

Citations Cited by
17
The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies
The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies
Material Type:
Article 		Add to My Research

The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies

Molecular cytogenetics, 2018-12, Vol.11 (1), p.59-59, Article 59 [Peer Reviewed Journal]

COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. This work is licensed 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. ;The Author(s). 2018 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-018-0407-z ;PMID: 30524505

Full text available

Citations Cited by
18
Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018-2020: A Retrospective Analysis
Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018-2020: A Retrospective Analysis
Material Type:
Article 		Add to My Research

Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018-2020: A Retrospective Analysis

Journal of personalized medicine, 2022-01, Vol.12 (1), p.48 [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: 2075-4426 ;EISSN: 2075-4426 ;DOI: 10.3390/jpm12010048 ;PMID: 35055363

Full text available

Citations Cited by
19
Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women
Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women
Material Type:
Article 		Add to My Research

Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women

Iranian journal of public health, 2019-01, Vol.48 (1), p.126-131 [Peer Reviewed Journal]

2019. This work is published under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright© Iranian Public Health Association & Tehran University of Medical Sciences 2019 ;ISSN: 2251-6085 ;EISSN: 2251-6093 ;DOI: 10.18502/ijph.v48i1.791 ;PMID: 30847320

Full text available

Citations Cited by
20
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience
Material Type:
Article 		Add to My Research

Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience

BMC research notes, 2020-03, Vol.13 (1), p.167-167, Article 167 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed 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. ;The Author(s) 2020 ;ISSN: 1756-0500 ;EISSN: 1756-0500 ;DOI: 10.1186/s13104-020-05009-1 ;PMID: 32188487

Full text available

Citations Cited by

Results 1 - 20 of 385  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 1977  (10)
  2. 1977 To 1988  (14)
  3. 1989 To 2002  (12)
  4. 2003 To 2012  (59)
  5. After 2012  (291)
  6. More options open sub menu

Language 

  1. English  (380)
  2. Japanese  (34)
  3. German  (5)
  4. French  (4)
  5. Portuguese  (2)
  6. Russian  (1)
  7. Swedish  (1)
  8. Danish  (1)
  9. Italian  (1)
  10. Norwegian  (1)
  11. Afrikaans  (1)
  12. Chinese  (1)
  13. Spanish  (1)
  14. 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