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Results 1 - 20 of 615  for All Library Resources

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Refined by: subject: Female remove subject: Medical Sciences remove xxx: xxx remove
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1
Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY
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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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2
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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3
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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4
Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee
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Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee

Clinical and experimental rheumatology, 2010-11, Vol.28 (6), p.803-805 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0392-856X ;EISSN: 1593-098X ;PMID: 21205458

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5
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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6
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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7
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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8
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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9
Female-to-male transsexual with 47,XXX karyotype
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Female-to-male transsexual with 47,XXX karyotype

Biological psychiatry (1969), 2000-12, Vol.48 (11), p.1116-1117 [Peer Reviewed Journal]

2000 Society of Biological Psychiatry ;2001 INIST-CNRS ;ISSN: 0006-3223 ;EISSN: 1873-2402 ;DOI: 10.1016/S0006-3223(00)00954-9 ;PMID: 11094147 ;CODEN: BIPCBF

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10
Spontaneous pregnancy in a woman with 45,X/47,XXX mosaicism in both serum and germ cell lines. A case report
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Spontaneous pregnancy in a woman with 45,X/47,XXX mosaicism in both serum and germ cell lines. A case report

Journal of reproductive medicine, 2003-02, Vol.48 (2), p.121 [Peer Reviewed Journal]

ISSN: 0024-7758 ;EISSN: 1943-3565 ;PMID: 12621797

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11
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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Doctors’ experiences of adverse events in secondary care: the professional and personal impact

Clinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Peer Reviewed Journal]

2014 © 2014 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;2015 INIST-CNRS ;2014 Royal College of Physicians. ;2014 Royal College of Physicians 2014 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.14-6-585 ;PMID: 25468840

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12
Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty
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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

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13
The parental origin of the extra X chromosome in 47,XXX females
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The parental origin of the extra X chromosome in 47,XXX females

American journal of human genetics, 1990-04, Vol.46 (4), p.754-761 [Peer Reviewed Journal]

1991 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 2316522 ;CODEN: AJHGAG

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14
Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21

Journal of medical genetics, 1995-08, Vol.32 (8), p.650-653 [Peer Reviewed Journal]

1995 INIST-CNRS ;Copyright BMJ Publishing Group LTD Aug 1995 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.32.8.650 ;PMID: 7473661 ;CODEN: JMDGAE

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15
Neurofibromatosis complicated with XXX syndrome and renovascular hypertension
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Neurofibromatosis complicated with XXX syndrome and renovascular hypertension

Journal of internal medicine, 1996-06, Vol.239 (6), p.531-535 [Peer Reviewed Journal]

Blackwell Science Ltd ;1996 INIST-CNRS ;ISSN: 0954-6820 ;EISSN: 1365-2796 ;DOI: 10.1046/j.1365-2796.1996.422778000.x ;PMID: 8656147

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16
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis
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Article
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Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis

European journal of pediatrics, 2010-10, Vol.169 (10), p.1255-1261 [Peer Reviewed Journal]

Springer-Verlag 2010 ;2015 INIST-CNRS ;ISSN: 0340-6199 ;EISSN: 1432-1076 ;DOI: 10.1007/s00431-010-1221-8 ;PMID: 20473517 ;CODEN: EJPEDT

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17
Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester
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Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester

Fetal diagnosis and therapy, 2000-03, Vol.15 (2), p.97-101 [Peer Reviewed Journal]

2000 S. Karger AG, Basel ;2000 INIST-CNRS ;Copyright 2000 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874

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18
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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19
Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorion
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Article
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Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: Mosaicism confirmed in cord blood, amnion, and chorion

Prenatal diagnosis, 1992-12, Vol.12 (12), p.1043-1046 [Peer Reviewed Journal]

Copyright © 1992 John Wiley & Sons, Ltd. ;1993 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970121210 ;PMID: 1283786 ;CODEN: PRDIDM

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20
Monozygotic Twinning in a Female with Triple X [47, XXX]
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Monozygotic Twinning in a Female with Triple X [47, XXX]

Gynecologic and obstetric investigation, 1994, Vol.37 (4), p.279-280 [Peer Reviewed Journal]

1994 S. Karger AG, Basel ;1994 INIST-CNRS ;ISSN: 0378-7346 ;EISSN: 1423-002X ;DOI: 10.1159/000292578 ;PMID: 8050736 ;CODEN: GOBIDS

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