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1
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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2
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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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

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3
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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4
A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention
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A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention

Clinical genetics, 2020-01, Vol.97 (1), p.156 [Peer Reviewed Journal]

2019 The Authors. Clinical Genetics published by John Wiley & Sons Ltd. ;EISSN: 1399-0004 ;DOI: 10.1111/cge.13586 ;PMID: 31267526

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5
Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature
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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. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426

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6
47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation
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47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation

American journal of medical genetics, 1988-03, Vol.29 (3), p.511-515 [Peer Reviewed Journal]

Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company ;1989 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320290306 ;PMID: 3376994 ;CODEN: AJMGDA

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7
A case of liveborn triploidy (69,XXX)
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A case of liveborn triploidy (69,XXX)

Acta pædiatrica Scandinavica, 1972-03, Vol.61 (2), p.203-208 [Peer Reviewed Journal]

ISSN: 0001-656X ;DOI: 10.1111/j.1651-2227.1972.tb15925.x ;PMID: 4622018

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8
Twin pregnancy in woman with 45,X/47,XXX karyotype
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Twin pregnancy in woman with 45,X/47,XXX karyotype

Obstetrics and gynecology (New York. 1953), 1980-09, Vol.56 (3), p.401 [Peer Reviewed Journal]

ISSN: 0029-7844 ;EISSN: 1873-233X ;PMID: 7422184

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9
A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY
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A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY

Human genetics, 1984-01, Vol.66 (4), p.367-369 [Peer Reviewed Journal]

1985 INIST-CNRS ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00287644 ;PMID: 6586638 ;CODEN: HUGEDQ

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10
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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11
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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12
Prenatal diagnosis of triploidy (69,XXX) in the 29th week of pregnancy with fetal death in the 37th week of pregnancy
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Prenatal diagnosis of triploidy (69,XXX) in the 29th week of pregnancy with fetal death in the 37th week of pregnancy

Zentralblatt für Gynäkologie, 1990, Vol.112 (1), p.49 [Peer Reviewed Journal]

ISSN: 0044-4197 ;PMID: 2316295

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13
Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man
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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

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14
Pregnancy in a woman having Turner syndrome with 45,X/46,XX/47,XXX mosaicism
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Pregnancy in a woman having Turner syndrome with 45,X/46,XX/47,XXX mosaicism

Medicina clínica, 1982-09, Vol.79 (4), p.189 [Peer Reviewed Journal]

ISSN: 0025-7753 ;PMID: 7144294

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15
Fertility in patients with 45,X/46, XX and 45,X/47,XXX mosaicism (author's transl)
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Fertility in patients with 45,X/46, XX and 45,X/47,XXX mosaicism (author's transl)

Ceskoslovenska gynekologie, 1982-06, Vol.47 (5), p.328

ISSN: 0374-6852 ;PMID: 7105204

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16
Is the prevalence of Klinefelter syndrome increasing?
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Is the prevalence of Klinefelter syndrome increasing?

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.163-170 [Peer Reviewed Journal]

2008 INIST-CNRS ;Copyright Nature Publishing Group Feb 2008 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201956 ;PMID: 18000523

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17
Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth
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Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birth

BMC women's health, 2024-01, Vol.24 (1), p.42-12, Article 42 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1472-6874 ;EISSN: 1472-6874 ;DOI: 10.1186/s12905-023-02856-5 ;PMID: 38225596

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18
Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancy
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Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancy

Ultrasound in obstetrics & gynecology, 2015-01, Vol.45 (1), p.55 [Peer Reviewed Journal]

Copyright © 2014 ISUOG. Published by John Wiley & Sons Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.13460 ;PMID: 25044397

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19
Breastfeeding at 1, 3 and 6 Months after Birth According to the Mode of Birth: A Correlation Study
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Breastfeeding at 1, 3 and 6 Months after Birth According to the Mode of Birth: A Correlation Study

International journal of environmental research and public health, 2020-09, Vol.17 (18), p.6828 [Peer Reviewed Journal]

2020 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 (http://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. ;2020 by the authors. 2020 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph17186828 ;PMID: 32962055

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20
Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome
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Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome

Prenatal diagnosis, 2010-11, Vol.30 (11), p.1072-1078 [Peer Reviewed Journal]

Copyright © 2010 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2613 ;PMID: 20842625 ;CODEN: PRDIDM

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