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 634  for All Library Resources

Results 1 2 3 4 5 next page
Show only
Refined by: resource type: Articles remove xxx: xxx remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
Material Type:
Article
Add to My Research

Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study

Prenatal diagnosis, 2016-06, Vol.36 (6), p.523-529 [Peer Reviewed Journal]

2016 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4817 ;PMID: 27018091

Full text available

2
Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcome
Material Type:
Article
Add to My Research

Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcome

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.906-909 [Peer Reviewed Journal]

ISSN: 1028-4559 ;DOI: 10.1016/j.tjog.2023.09.005

Full text available

3
45,X/46,XX at the first amniocentesis, and 45,X/47,XXX/46,XX at the repeat amniocentesis and at birth in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the 45,X cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes
Material Type:
Article
Add to My Research

45,X/46,XX at the first amniocentesis, and 45,X/47,XXX/46,XX at the repeat amniocentesis and at birth in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the 45,X cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.901-905 [Peer Reviewed Journal]

ISSN: 1028-4559 ;DOI: 10.1016/j.tjog.2023.09.004

Full text available

4
Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX
Material Type:
Article
Add to My Research

Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX

The journal of obstetrics and gynaecology research, 2014-01, Vol.40 (1), p.259-262 [Peer Reviewed Journal]

2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology ;2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology. ;ISSN: 1341-8076 ;EISSN: 1447-0756 ;DOI: 10.1111/jog.12131 ;PMID: 23937348

Full text available

5
Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus
Material Type:
Article
Add to My Research

Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus

Archives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Peer Reviewed Journal]

Springer-Verlag Berlin Heidelberg 2013 ;Archives of Gynecology and Obstetrics is a copyright of Springer, (2013). All Rights Reserved. ;ISSN: 0932-0067 ;EISSN: 1432-0711 ;DOI: 10.1007/s00404-013-2847-3 ;PMID: 23625330

Full text available

6
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation
Material Type:
Article
Add to My Research

Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation

Fertility and sterility, 2008-06, Vol.89 (6), p.1826.e5-1826.e7 [Peer Reviewed Journal]

American Society for Reproductive Medicine ;2008 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2007.06.065 ;PMID: 17953951

Full text available

7
47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development
Material Type:
Article
Add to My Research

47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development

Fertility and sterility, 2009-11, Vol.92 (5), p.1747.e5-1747.e7 [Peer Reviewed Journal]

American Society for Reproductive Medicine ;2009 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2009.07.1008 ;PMID: 19732877

Full text available

8
XXX Congreso Nacional de Obstetricia y Ginecología
Material Type:
Article
Add to My Research

XXX Congreso Nacional de Obstetricia y Ginecología

Revista obstetricia y ginecología de Venezuela, 2015-06, Vol.75 (2), p.138-143

ISSN: 0048-7732

Full text available

9
Diagnóstico prenatal de un feto con doble trisomía con cariotipo 48 XXX +18: reporte de un caso
Material Type:
Article
Add to My Research

Diagnóstico prenatal de un feto con doble trisomía con cariotipo 48 XXX +18: reporte de un caso

Ginecologia y obstetricia de Mexico, 2018-12, Vol.86 (12), p.810-814

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0300-9041 ;DOI: 10.24245/gom.v86i12.1814

Full text available

10
Trabajos ganadores presentados en el XXX Congreso Nacional de Obstetricia y Ginecología realizado del 25 al 28 de mayo de 2016 en Cali (Colombia)
Material Type:
Article
Add to My Research

Trabajos ganadores presentados en el XXX Congreso Nacional de Obstetricia y Ginecología realizado del 25 al 28 de mayo de 2016 en Cali (Colombia)

Revista colombiana de obstetricia y ginecología, 2016-06, Vol.67 (2), p.159-161 [Peer Reviewed Journal]

COPYRIGHT 2016 Federacion Colombiana de Asociaciones de Obstetricia y Ginecologia (FECOLSOG) ;This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ;ISSN: 0034-7434 ;ISSN: 2463-0225 ;EISSN: 2463-0225 ;DOI: 10.18597/rcog.382

Full text available

11
Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases
Material Type:
Article
Add to My Research

Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases

Prenatal 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: 15614873

Full text available

12
Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature
Material Type:
Article
Add to My Research

Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature

Fetal diagnosis and therapy, 2010-03, Vol.27 (2), p.113-117 [Peer Reviewed Journal]

2010 S. Karger AG, Basel ;2015 INIST-CNRS ;2010 S. Karger AG, Basel. ;Copyright (c) 2010 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426

Full text available

13
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

14
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
Material Type:
Article
Add to My Research

Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Peer Reviewed Journal]

Copyright © 2000 John Wiley & Sons, Ltd. ;Copyright 2000 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E ;PMID: 11015706

Full text available

15
Prenatal diagnosis and prognosis of triple&#160;X syndrome: 47,&#160;XXX
Material Type:
Article
Add to My Research

Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX

Journal de gynécologie, obstétrique et biologie de la reproduction, 2009-11, Vol.38 (7), p.599-603

2009 Elsevier Masson SAS ;2009 INIST-CNRS ;ISSN: 0368-2315 ;DOI: 10.1016/j.jgyn.2009.08.003 ;PMID: 19762167 ;CODEN: JGOBAC

Full text available

16
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
Material Type:
Article
Add to My Research

Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Peer Reviewed Journal]

2000 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E ;CODEN: PRDIDM

Full text available

17
Serum screening in complete triploidy 69,XXX
Material Type:
Article
Add to My Research

Serum screening in complete triploidy 69,XXX

Prenatal diagnosis, 1996-06, Vol.16 (6), p.578 [Peer Reviewed Journal]

ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/(SICI)1097-0223(199606)16:6<578::AID-PD891>3.0.CO;2-N ;PMID: 8809905

Full text available

18
Inter-observer discrepancy in scoring signals on interphase fish with an X library probe illustrated in a case of 47, XXX
Material Type:
Article
Add to My Research

Inter-observer discrepancy in scoring signals on interphase fish with an X library probe illustrated in a case of 47, XXX

Prenatal diagnosis, 1995-12, Vol.15 (12), p.1193-1195 [Peer Reviewed Journal]

Copyright © 1995 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970151221 ;PMID: 8750305

Full text available

19
Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester
Material Type:
Article
Add to My Research

Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester

Fetal diagnosis and therapy, 2000-03, Vol.15 (2), p.97-101 [Peer Reviewed Journal]

2000 S. Karger AG, Basel ;2000 INIST-CNRS ;Copyright 2000 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874

Full text available

20
Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorion
Material Type:
Article
Add to My Research

Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorion

Prenatal diagnosis, 1992-12, Vol.12 (12), p.1043-1046 [Peer Reviewed Journal]

Copyright © 1992 John Wiley & Sons, Ltd. ;1993 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970121210 ;PMID: 1283786 ;CODEN: PRDIDM

Full text available

Results 1 - 20 of 634  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (612)

Refine My Results

Creation Date 

From To
  1. Before 1987  (14)
  2. 1987 To 1996  (46)
  3. 1997 To 2005  (121)
  4. 2006 To 2015  (276)
  5. After 2015  (178)
  6. More options open sub menu

Language 

  1. English  (617)
  2. Japanese  (78)
  3. Portuguese  (23)
  4. Polish  (14)
  5. Spanish  (7)
  6. French  (4)
  7. German  (4)
  8. More options open sub menu

Searching Remote Databases, Please Wait