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1
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
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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

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2
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
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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

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3
Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX
Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX
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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

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4
Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX
Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX
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Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX

Birth defects research. A Clinical and molecular teratology, 2007-08, Vol.79 (8), p.612-613 [Peer Reviewed Journal]

Copyright © 2007 Wiley‐Liss, Inc. ;2007 Wiley-Liss, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.20371 ;PMID: 17469201

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5
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)
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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: 12848653

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6
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
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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

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7
Prenatal diagnosis and prognosis of triple&#160;X syndrome: 47,&#160;XXX
Prenatal diagnosis and prognosis of triple&#160;X syndrome: 47,&#160;XXX
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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

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8
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis
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Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis

European journal of pediatrics, 2010-10, Vol.169 (10), p.1255-1261 [Peer Reviewed Journal]

Springer-Verlag 2010 ;2015 INIST-CNRS ;ISSN: 0340-6199 ;EISSN: 1432-1076 ;DOI: 10.1007/s00431-010-1221-8 ;PMID: 20473517 ;CODEN: EJPEDT

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9
Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorion
Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorion
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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

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10
45,X/46,XX/47,XXX phenotype
45,X/46,XX/47,XXX phenotype
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45,X/46,XX/47,XXX phenotype

Prenatal diagnosis, 1993-12, Vol.13 (12), p.1165-1166 [Peer Reviewed Journal]

Copyright © 1993 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970131219 ;PMID: 8177840

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11
Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities
Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities
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Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities

American journal of medical genetics, 2002-06, Vol.110 (1), p.11-18 [Peer Reviewed Journal]

Copyright © 2002 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2002 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.10394 ;PMID: 12116265 ;CODEN: AJMGDA

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12
Evidence of a second gamete fusion after the first cleavage of the zygote in a 47,XX, + 18/70,XXX, + 18 mosaic. A remarkable diploid-triploid discrepancy after CVS
Evidence of a second gamete fusion after the first cleavage of the zygote in a 47,XX, + 18/70,XXX, + 18 mosaic. A remarkable diploid-triploid discrepancy after CVS
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Evidence of a second gamete fusion after the first cleavage of the zygote in a 47,XX, + 18/70,XXX, + 18 mosaic. A remarkable diploid-triploid discrepancy after CVS

Prenatal diagnosis, 1993-04, Vol.13 (4), p.301-306 [Peer Reviewed Journal]

Copyright © 1993 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970130409 ;PMID: 8506231

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13
Prenatal diagnosis and gonadal findings in X/XXX mosaicism
Prenatal diagnosis and gonadal findings in X/XXX mosaicism
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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

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14
Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies
Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies
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Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies

American journal of medical genetics, 1998-12, Vol.80 (4), p.330-334 [Peer Reviewed Journal]

Copyright © 1998 Wiley‐Liss, Inc. ;1999 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/(SICI)1096-8628(19981204)80:4<330::AID-AJMG6>3.0.CO;2-7 ;PMID: 9856559 ;CODEN: AJMGDA

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15
Antenatal diagnosis of an XXX female. A dilemma for genetic counseling
Antenatal diagnosis of an XXX female. A dilemma for genetic counseling
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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

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16
Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus
Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus
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Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus

American journal of medical genetics, 1989-06, Vol.33 (2), p.242-243 [Peer Reviewed Journal]

Copyright © 1989 Wiley‐Liss, Inc., A Wiley Company ;1989 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320330220 ;PMID: 2669483 ;CODEN: AJMGDA

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17
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
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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

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18
Prenatal Diagnosis of Congenital Diaphragmatic Hernia in a McFadden Kalousek Type 2 Triploid Fetus
Prenatal Diagnosis of Congenital Diaphragmatic Hernia in a McFadden Kalousek Type 2 Triploid Fetus
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Prenatal Diagnosis of Congenital Diaphragmatic Hernia in a McFadden Kalousek Type 2 Triploid Fetus

Fetal diagnosis and therapy, 2004-01, Vol.19 (1), p.49-51 [Peer Reviewed Journal]

2004 S. Karger AG, Basel ;2004 INIST-CNRS ;Copyright 2004 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000074260 ;PMID: 14646418

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19
Letter: Possible mosaic XXX-XXY marriage with abnormal offspring
Letter: Possible mosaic XXX-XXY marriage with abnormal offspring
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Letter: Possible mosaic XXX-XXY marriage with abnormal offspring

The Lancet (British edition), 1975-02, Vol.1 (7902), p.334-334 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 46475

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20
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
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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

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