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Results 1 - 20 of 466  for All Library Resources

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Refined by: subject: Adolescent remove subject: Female remove xxx: xxx remove
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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
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome

Genes, brain and behavior, 2014-11, Vol.13 (8), p.841-849 [Peer Reviewed Journal]

Published 2014. This article is a U.S. Government work and is in the public domain in the USA. ;2014 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12180 ;PMID: 25287572 ;CODEN: GBBEAO

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3
Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY
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Article
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Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY

Journal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309 [Peer Reviewed Journal]

EISSN: 1536-7312 ;DOI: 10.1097/DBP.0b013e31824501c8 ;PMID: 22333574

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4
Mortality and incidence in women with 47,XXX and variants
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Mortality and incidence in women with 47,XXX and variants

American journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Peer Reviewed Journal]

Copyright © 2010 Wiley‐Liss, Inc. ;Copyright 2010 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.33214 ;PMID: 20101696

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5
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
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Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2870-2881 [Peer Reviewed Journal]

2016 Wiley Periodicals, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.37688 ;PMID: 27644018

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6
Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)
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Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)

Acta odontologica Scandinavica, 2010-07, Vol.68 (4), p.223 [Peer Reviewed Journal]

EISSN: 1502-3850 ;DOI: 10.3109/00016357.2010.490954 ;PMID: 20568965

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7
A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention
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Article
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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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8
Validation of an Objective Assessment Tool for Tonsillectomy in Otolaryngology Resident Training
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Article
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Validation of an Objective Assessment Tool for Tonsillectomy in Otolaryngology Resident Training

The Laryngoscope, 2021-02, Vol.131 (2), p.E359 [Peer Reviewed Journal]

2020 The American Laryngological, Rhinological and Otological Society, Inc. ;EISSN: 1531-4995 ;DOI: 10.1002/lary.28739 ;PMID: 32510606

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9
Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXX
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Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXX

Journal of the American Academy of Child and Adolescent Psychiatry, 1998-03, Vol.37 (3), p.286-291 [Peer Reviewed Journal]

1998 The American Academy of Child and Adolescent Psychiatry ;1998 INIST-CNRS ;Copyright Lippincott Williams & Wilkins Mar 1998 ;ISSN: 0890-8567 ;EISSN: 1527-5418 ;DOI: 10.1097/00004583-199803000-00013 ;PMID: 9519633 ;CODEN: JAAPEE

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10
47,XXX: what is the prognosis?
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47,XXX: what is the prognosis?

Pediatrics (Evanston), 1988-10, Vol.82 (4), p.619-630 [Peer Reviewed Journal]

ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.82.4.619 ;PMID: 2459656

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11
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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Article
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome

Genes Brain & Behavior, 2014-11, Vol.13 (8), p.841-849

public

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12
The growth of XXX females: population-based studies
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Article
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The growth of XXX females: population-based studies

Annals of human biology, 1994, Vol.21 (1), p.57-66 [Peer Reviewed Journal]

1994 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1994 ;1994 INIST-CNRS ;ISSN: 0301-4460 ;EISSN: 1464-5033 ;DOI: 10.1080/03014469400003072 ;PMID: 8147577 ;CODEN: AHUBBJ

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13
Sports-related maxillofacial fractures: a retrospective study of 125 patients
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Article
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Sports-related maxillofacial fractures: a retrospective study of 125 patients

International journal of oral and maxillofacial surgery, 2005-09, Vol.34 (6), p.635 [Peer Reviewed Journal]

ISSN: 0901-5027 ;EISSN: 1399-0020 ;DOI: 10.1016/j.ijom.2005.01.008 ;PMID: 16053888

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14
Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities
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Article
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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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15
Fertility issues and pregnancy outcomes in Turner syndrome
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Article
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Fertility issues and pregnancy outcomes in Turner syndrome

Fertility and sterility, 2020-07, Vol.114 (1), p.144-154 [Peer Reviewed Journal]

2020 American Society for Reproductive Medicine ;Copyright © 2020 American Society for Reproductive Medicine. All rights reserved. ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2020.03.002 ;PMID: 32622407

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16
Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital
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Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital

Ultrasound in obstetrics & gynecology, 2014-07, Vol.44 (1), p.17 [Peer Reviewed Journal]

Copyright © 2014 ISUOG. Published by John Wiley & Sons Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.13361 ;PMID: 24616044

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17
Liver biochemical abnormalities in Turner syndrome: A comprehensive characterization of an adult population
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Article
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Liver biochemical abnormalities in Turner syndrome: A comprehensive characterization of an adult population

Clinical endocrinology (Oxford), 2018-11, Vol.89 (5), p.667 [Peer Reviewed Journal]

2018 John Wiley & Sons Ltd. ;EISSN: 1365-2265 ;DOI: 10.1111/cen.13811 ;PMID: 29992593

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18
An assessment of the analytical performance of non‐invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717‐patient sample in a single prenatal diagnosis Centre in China
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An assessment of the analytical performance of non‐invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717‐patient sample in a single prenatal diagnosis Centre in China

The journal of gene medicine, 2021-09, Vol.23 (9), p.e3362-n/a [Peer Reviewed Journal]

2021 John Wiley & Sons, Ltd. ;ISSN: 1099-498X ;EISSN: 1521-2254 ;DOI: 10.1002/jgm.3362 ;PMID: 33973298

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19
Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in Iran
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Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in Iran

Fetal diagnosis and therapy, 2020-03, Vol.47 (3), p.220-227 [Peer Reviewed Journal]

2019 S. Karger AG, Basel ;2019 S. Karger AG, Basel. ;COPYRIGHT 2020 S. Karger AG ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000501014 ;PMID: 31487708

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20
The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes
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Article
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The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes

Journal of assisted reproduction and genetics, 2022-05, Vol.39 (5), p.1143-1153 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 ;2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. ;The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022. ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-022-02469-1 ;PMID: 35320443

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