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1	Material Type: Article	Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review Developmental medicine and child neurology, 2010-02, Vol.52 (2), p.119-129 [Peer Reviewed Journal] The Authors. Journal compilation © Mac Keith Press 2010 ;Copyright Mac Keith Press Feb 2010 ;Copyright © 2010 Mac Keith Press ;ISSN: 0012-1622 ;EISSN: 1469-8749 ;DOI: 10.1111/j.1469-8749.2009.03545.x ;PMID: 20059514 ;CODEN: DMCNAW Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	Material Type: Article	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 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
3	Material Type: Article	Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX Genes, brain and behavior, 2015-02, Vol.14 (2), p.200-208 [Peer Reviewed Journal] 2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society ;2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society. ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12203 ;PMID: 25684214 ;CODEN: GBBEAO Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	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 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty The Journal of pediatrics, 2001-11, Vol.139 (5), p.724-728 [Peer Reviewed Journal] 2001 Mosby, Inc. ;2002 INIST-CNRS ;ISSN: 0022-3476 ;EISSN: 1097-6833 ;DOI: 10.1067/mpd.2001.118571 ;PMID: 11713453 ;CODEN: JOPDAB Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
6	Material Type: Article	45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism American journal of medical genetics. Part A, 2004-10, Vol.130A (3), p.311-314 [Peer Reviewed Journal] Copyright © 2004 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.30258 ;PMID: 15378545 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
7	Material Type: Article	47,XXX male: A clinical and molecular study American journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Peer Reviewed Journal] Copyright © 2001 Wiley‐Liss, Inc. ;2001 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/1096-8628(20010201)98:4<353::AID-AJMG1110>3.0.CO;2-D ;PMID: 11170081 ;CODEN: AJMGDA Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
8	Material Type: Article	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 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction Human genetics, 1989-02, Vol.81 (3), p.247-251 [Peer Reviewed Journal] 1989 INIST-CNRS ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00278998 ;PMID: 2921034 ;CODEN: HUGEDQ Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
10	Material Type: Article	Verbal deficits in children with 47, XXY and 47, XXX karyotypes: A descriptive and experimental study Brain and language, 1982-09, Vol.17 (1), p.58-72 [Peer Reviewed Journal] 1982 ;ISSN: 0093-934X ;EISSN: 1090-2155 ;DOI: 10.1016/0093-934X(82)90005-0 ;PMID: 7139271 ;CODEN: BRLGAZ Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
11	Material Type: Article	The dermatoglyphics of a Toronto sample of children with XXY, XXYY, and XXX aneuploidies American journal of physical anthropology, 1980-01, Vol.52 (1), p.33-41 [Peer Reviewed Journal] Copyright © 1980 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0002-9483 ;EISSN: 1096-8644 ;DOI: 10.1002/ajpa.1330520106 ;PMID: 7369334 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	XXY son of XX-XXX mother The Lancet (British edition), 1972-04, Vol.1 (7757), p.955-955 [Peer Reviewed Journal] ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4112113 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
13	Material Type: Article	De subitaneis mortibus. XXX. Observations on the pathophysiology of the long QT syndromes with special reference to the neuropathology of the heart Circulation (New York, N.Y.), 1978-06, Vol.57 (6), p.1221-1231 [Peer Reviewed Journal] ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/01.CIR.57.6.1221 ;PMID: 639246 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
14	Material Type: Article	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 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
15	Material Type: Article	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 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesis Acta Paediatrica, 2011-06, Vol.100 (6), p.903-907 [Peer Reviewed Journal] 2011 The Author(s)/Acta Pædiatrica © 2011 Foundation Acta Pædiatrica ;2015 INIST-CNRS ;2011 The Author(s)/Acta Paediatrica © 2011 Foundation Acta Paediatrica. ;Acta Pædiatrica © 2011 Foundation Acta Pædiatrica 2011 ;ISSN: 0803-5253 ;EISSN: 1651-2227 ;DOI: 10.1111/j.1651-2227.2011.02150.x ;PMID: 21418292 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
17	Material Type: Article	“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies Journal of genetic counseling, 2015-02, Vol.24 (1), p.88-103 [Peer Reviewed Journal] National Society of Genetic Counselors, Inc. 2014 ;2015 National Society of Genetic Counselors, Inc. ;National Society of Genetic Counselors, Inc. 2015 ;ISSN: 1059-7700 ;EISSN: 1573-3599 ;DOI: 10.1007/s10897-014-9741-4 ;PMID: 25179748 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
18	Material Type: Article	Evaluating Pediatric Ophthalmic Care Using Sentiment Analysis of Physician Review Sites Journal of pediatric ophthalmology and strabismus, 2024-05, Vol.61 (3), p.211-8 [Peer Reviewed Journal] COPYRIGHT 2024 Slack, Inc. ;Copyright 2024, SLACK Incorporated ;ISSN: 0191-3913 ;EISSN: 1938-2405 ;DOI: 10.3928/01913913-20240108-01 ;PMID: 38275203 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	Which neurodevelopmental disorders get researched and why? PloS one, 2010-11, Vol.5 (11), p.e15112 [Peer Reviewed Journal] COPYRIGHT 2010 Public Library of Science ;COPYRIGHT 2010 Public Library of Science ;2010 Dorothy V. M. Bishop. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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. ;Dorothy V. M. Bishop. 2010 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0015112 ;PMID: 21152085 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
20	Material Type: Article	Prevalence of adolescent idiopathic scoliosis in Shijiazhuang, Hebei, China: a cross-sectional study European spine journal, 2024-02, Vol.33 (2), p.673-679 [Peer Reviewed Journal] The Author(s) 2023 ;2023. The Author(s). ;The Author(s) 2023. This work is published 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. ;ISSN: 0940-6719 ;EISSN: 1432-0932 ;DOI: 10.1007/s00586-023-08030-7 ;PMID: 38006475 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by

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Results 1 - 20 of 447 for All Library Resources

The Authors. Journal compilation © Mac Keith Press 2010 ;Copyright Mac Keith Press Feb 2010 ;Copyright © 2010 Mac Keith Press ;ISSN: 0012-1622 ;EISSN: 1469-8749 ;DOI: 10.1111/j.1469-8749.2009.03545.x ;PMID: 20059514 ;CODEN: DMCNAW

2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society ;2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society. ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12203 ;PMID: 25684214 ;CODEN: GBBEAO

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

2001 Mosby, Inc. ;2002 INIST-CNRS ;ISSN: 0022-3476 ;EISSN: 1097-6833 ;DOI: 10.1067/mpd.2001.118571 ;PMID: 11713453 ;CODEN: JOPDAB

Copyright © 2004 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.30258 ;PMID: 15378545

Copyright © 2001 Wiley‐Liss, Inc. ;2001 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/1096-8628(20010201)98:4<353::AID-AJMG1110>3.0.CO;2-D ;PMID: 11170081 ;CODEN: AJMGDA

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

1989 INIST-CNRS ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00278998 ;PMID: 2921034 ;CODEN: HUGEDQ

1982 ;ISSN: 0093-934X ;EISSN: 1090-2155 ;DOI: 10.1016/0093-934X(82)90005-0 ;PMID: 7139271 ;CODEN: BRLGAZ

Copyright © 1980 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0002-9483 ;EISSN: 1096-8644 ;DOI: 10.1002/ajpa.1330520106 ;PMID: 7369334

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4112113

ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/01.CIR.57.6.1221 ;PMID: 639246

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

National Society of Genetic Counselors, Inc. 2014 ;2015 National Society of Genetic Counselors, Inc. ;National Society of Genetic Counselors, Inc. 2015 ;ISSN: 1059-7700 ;EISSN: 1573-3599 ;DOI: 10.1007/s10897-014-9741-4 ;PMID: 25179748

COPYRIGHT 2024 Slack, Inc. ;Copyright 2024, SLACK Incorporated ;ISSN: 0191-3913 ;EISSN: 1938-2405 ;DOI: 10.3928/01913913-20240108-01 ;PMID: 38275203

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