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1
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study

Orphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 2019. 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). 2019 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-018-0976-2 ;PMID: 30642344

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2
Long-term survival in a 69,XXX triploid premature infant
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Long-term survival in a 69,XXX triploid premature infant

American journal of medical genetics. Part A, 2008-06, Vol.146A (12), p.1618-1621 [Peer Reviewed Journal]

Copyright © 2008 Wiley‐Liss, Inc. ;2008 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.32352 ;PMID: 18478596

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3
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

American journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Peer Reviewed Journal]

Copyright © 2001 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.10154 ;PMID: 11840512 ;CODEN: AJMGDA

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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
Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals
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Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals

Medical journal of Australia, 1983-11, Vol.2 (11), p.535 [Peer Reviewed Journal]

ISSN: 0025-729X ;EISSN: 1326-5377 ;DOI: 10.5694/j.1326-5377.1983.tb122644.x ;PMID: 6633377

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6
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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7
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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8
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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9
A Livebirth with Triploidy Syndrome (69,XXX)
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A Livebirth with Triploidy Syndrome (69,XXX)

Clinical pediatrics, 1981-12, Vol.20 (12), p.806-807 [Peer Reviewed Journal]

ISSN: 0009-9228 ;EISSN: 1938-2707 ;DOI: 10.1177/000992288102001210 ;PMID: 7307419

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10
Triploidy syndrome: A report on two live-born (69, XXY) and one still-born (69, XXX) infants
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Triploidy syndrome: A report on two live-born (69, XXY) and one still-born (69, XXX) infants

Clinical genetics, 1976-01, Vol.9 (1), p.43-50 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1976.tb01548.x ;PMID: 174849

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11
Lattice degeneration of the retina. XXX Edward Jackson Memorial Lecture
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Lattice degeneration of the retina. XXX Edward Jackson Memorial Lecture

American journal of ophthalmology, 1974-05, Vol.77 (5), p.619 [Peer Reviewed Journal]

ISSN: 0002-9394 ;EISSN: 1879-1891 ;DOI: 10.1016/0002-9394(74)90525-X ;PMID: 4823775

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12
Surface Structure of Hairs in a Triploid (69,XXX) Individual
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Surface Structure of Hairs in a Triploid (69,XXX) Individual

Journal of investigative dermatology, 1974-10, Vol.63 (4), p.334-336 [Peer Reviewed Journal]

1974 The Williams & Wilkins Co. ;ISSN: 0022-202X ;EISSN: 1523-1747 ;DOI: 10.1111/1523-1747.ep12680326 ;PMID: 4417536

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13
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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14
Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes
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Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes

Birth defects original article series, 1979, Vol.15 (1), p.261

ISSN: 0547-6844 ;PMID: 444644

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15
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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16
Triploidy (69, and XXY and 69, XXX) in 2 newborn infants
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Triploidy (69, and XXY and 69, XXX) in 2 newborn infants

Verhandlungen der Deutschen Gesellschaft fur Pathologie, 1978, Vol.62, p.532

ISSN: 0070-4113 ;PMID: 746968

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17
Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study
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Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study

The Lancet. Psychiatry, 2023-02, Vol.10 (2), p.129 [Peer Reviewed Journal]

Copyright © 2023 Elsevier Ltd. All rights reserved. ;EISSN: 2215-0374 ;DOI: 10.1016/S2215-0366(23)00004-4 ;PMID: 36697121

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18
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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19
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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20
Breastfeeding in Spain and the factors related to its establishment and maintenance: LAyDI Study (PAPenRed)
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Breastfeeding in Spain and the factors related to its establishment and maintenance: LAyDI Study (PAPenRed)

Atención primaria, 2024-01, Vol.56 (1), p.102772-102772 [Peer Reviewed Journal]

Copyright © 2023 The Authors. Publicado por Elsevier España, S.L.U. All rights reserved. ;EISSN: 1578-1275 ;DOI: 10.1016/j.aprim.2023.102772 ;PMID: 37741187

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