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1
Generation XXX: Pornography Acceptance and Use among Emerging Adults
Generation XXX: Pornography Acceptance and Use among Emerging Adults
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Generation XXX: Pornography Acceptance and Use among Emerging Adults

Journal of adolescent research, 2008, Vol.23 (1), p.6 [Peer Reviewed Journal]

ISSN: 0743-5584 ;EISSN: 1552-6895 ;DOI: 10.1177/0743558407306348

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2
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

Human molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/3.8.1365 ;PMID: 7987316

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3
Prenatal diagnosis of 47,XXX
Prenatal diagnosis of 47,XXX
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Prenatal diagnosis of 47,XXX

American journal of obstetrics and gynecology, 2005-05, Vol.192 (5), p.1469 [Peer Reviewed Journal]

ISSN: 0002-9378 ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2004.12.037 ;PMID: 15902140

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4
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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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5
Pharmacological Properties of Traditional Medicine (XXX): Effects of Gyokuheifusan (玉屏風散) on Murine Antigen-Specific Antibody Production
Pharmacological Properties of Traditional Medicine (XXX): Effects of Gyokuheifusan (玉屏風散) on Murine Antigen-Specific Antibody Production
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Pharmacological Properties of Traditional Medicine (XXX): Effects of Gyokuheifusan (玉屏風散) on Murine Antigen-Specific Antibody Production

Biological and Pharmaceutical Bulletin, 2005, Vol.28(1), pp.110-113 [Peer Reviewed Journal]

2005 The Pharmaceutical Society of Japan ;ISSN: 0918-6158 ;EISSN: 1347-5215 ;DOI: 10.1248/bpb.28.110 ;PMID: 15635173

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6
Long-term survival in a 69,XXX triploid premature infant
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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7
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation
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Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation

Fertility and sterility, 2008-06, Vol.89 (6), p.1826.e5-1826.e7 [Peer Reviewed Journal]

American Society for Reproductive Medicine ;2008 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2007.06.065 ;PMID: 17953951

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8
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events

Rheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Peer Reviewed Journal]

2005 INIST-CNRS ;Copyright Oxford University Press(England) Jul 2005 ;ISSN: 1462-0324 ;EISSN: 1462-0332 ;DOI: 10.1093/rheumatology/keh613 ;PMID: 15797975 ;CODEN: BJRHDF

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9
The craniofacial complex in 47, XXX females
The craniofacial complex in 47, XXX females
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The craniofacial complex in 47, XXX females

European journal of orthodontics, 2005-08, Vol.27 (4), p.396-401 [Peer Reviewed Journal]

ISSN: 0141-5387 ;EISSN: 1460-2210 ;DOI: 10.1093/ejo/cji016 ;PMID: 16043476 ;CODEN: EJOODK

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10
Partial epilepsy and 47,XXX karyotype: report of four cases
Partial epilepsy and 47,XXX karyotype: report of four cases
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Partial epilepsy and 47,XXX karyotype: report of four cases

Pediatric neurology, 2006-07, Vol.35 (1), p.69 [Peer Reviewed Journal]

ISSN: 0887-8994 ;EISSN: 1873-5150 ;DOI: 10.1016/j.pediatrneurol.2006.01.003 ;PMID: 16814091

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11
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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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12
47,XXX associated with malformations
47,XXX associated with malformations
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47,XXX associated with malformations

American journal of medical genetics. Part A, 2004-02, Vol.125A (1), p.108-111 [Peer Reviewed Journal]

Copyright © 2003 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20393 ;PMID: 14755479

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13
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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14
Long survival in a 69,XXX triploid infant in Greece
Long survival in a 69,XXX triploid infant in Greece
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Long survival in a 69,XXX triploid infant in Greece

Genetics and molecular research, 2005-12, Vol.4 (4), p.755-759 [Peer Reviewed Journal]

ISSN: 1676-5680 ;EISSN: 1676-5680 ;PMID: 16475122

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15
Kallmann syndrome in a 47,XXX patient
Kallmann syndrome in a 47,XXX patient
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Kallmann syndrome in a 47,XXX patient

American journal of medical genetics. Part A, 2005-11, Vol.139A (1), p.52-53 [Peer Reviewed Journal]

Copyright © 2005 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.30996 ;PMID: 16222664

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16
Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India
Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India

Journal of genetics, 2008-12, Vol.87 (3), p.257-259 [Peer Reviewed Journal]

Indian Academy of Sciences 2008 ;ISSN: 0022-1333 ;EISSN: 0973-7731 ;DOI: 10.1007/s12041-008-0039-x ;PMID: 19147910

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17
Comparison of iron oxide labeling properties of hematopoietic progenitor cells from umbilical cord blood and from peripheral blood for subsequent in vivo tracking in a xenotransplant mouse model XXX
Comparison of iron oxide labeling properties of hematopoietic progenitor cells from umbilical cord blood and from peripheral blood for subsequent in vivo tracking in a xenotransplant mouse model XXX
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Comparison of iron oxide labeling properties of hematopoietic progenitor cells from umbilical cord blood and from peripheral blood for subsequent in vivo tracking in a xenotransplant mouse model XXX

Academic radiology, 2005-04, Vol.12 (4), p.502 [Peer Reviewed Journal]

ISSN: 1076-6332 ;EISSN: 1878-4046 ;DOI: 10.1016/j.acra.2004.12.021 ;PMID: 15831425

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18
Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases
Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases

Prenatal diagnosis, 2004-12, Vol.24 (12), p.1020-1021 [Peer Reviewed Journal]

Copyright © 2004 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1047 ;PMID: 15614873

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19
XXX syndrome
XXX syndrome
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XXX syndrome

Nihon rinshō, 2006-06, Vol.Suppl 2, p.522

ISSN: 0047-1852 ;PMID: 16817456

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20
Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXX
Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXX
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Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXX

Journal of gastroenterology, 2005-09, Vol.40 (9), p.914-916 [Peer Reviewed Journal]

Springer-Verlag Tokyo 2005 ;ISSN: 0944-1174 ;EISSN: 1435-5922 ;DOI: 10.1007/s00535-005-1659-z ;PMID: 16211352

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