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Results 1 - 20 of 1,515  for All Library Resources

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Refined by: creation date: 1991 To 2008 remove xxx: xxx remove
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1
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
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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
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
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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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
Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells
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Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells

Cytogenetic and genome research, 2004, Vol.104 (1-4), p.277-282 [Peer Reviewed Journal]

Copyright 2003 S. Karger AG, Basel ;ISSN: 1424-8581 ;EISSN: 1424-859X ;DOI: 10.1159/000077502 ;PMID: 15162051

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8
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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9
45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism
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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

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10
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
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Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX

Chromosome research, 2004-01, Vol.12 (2), p.125-132 [Peer Reviewed Journal]

Kluwer Academic Publishers 2004. ;ISSN: 0967-3849 ;EISSN: 1573-6849 ;DOI: 10.1023/B:CHRO.0000013164.56757.bd ;PMID: 15053482

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11
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Peer Reviewed Journal]

Copyright © 2000 John Wiley & Sons, Ltd. ;Copyright 2000 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E ;PMID: 11015706

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12
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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13
The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations
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The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations

Molecular biology and evolution, 1996-02, Vol.13 (2), p.314-323 [Peer Reviewed Journal]

ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/oxfordjournals.molbev.a025591 ;PMID: 8587497

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14
Azoospermia in a 46,xx/47,xxx phenotypic male
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Azoospermia in a 46,xx/47,xxx phenotypic male

Urology (Ridgewood, N.J.), 1996-12, Vol.48 (6), p.947-948 [Peer Reviewed Journal]

1996 Elsevier Science Inc. ;1997 INIST-CNRS ;ISSN: 0090-4295 ;EISSN: 1527-9995 ;DOI: 10.1016/S0090-4295(96)00321-4 ;PMID: 8973686 ;CODEN: URGYAZ

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15
47,XXX male: A clinical and molecular study
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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

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16
Normal growth and normalization of hypergonadotropic hypogonadism in atypical turner syndrome (45,X/46,XX/47,XXX) : correlation of body height with distribution of cell lines
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Article
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Normal growth and normalization of hypergonadotropic hypogonadism in atypical turner syndrome (45,X/46,XX/47,XXX) : correlation of body height with distribution of cell lines

European journal of pediatrics, 1994-06, Vol.153 (6), p.451-455 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0340-6199 ;EISSN: 1432-1076 ;DOI: 10.1007/BF01983411 ;PMID: 8088302 ;CODEN: EJPEDT

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17
Sports-related maxillofacial fractures: a retrospective study of 125 patients
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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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18
45,X/46,XX/47,XXX phenotype
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45,X/46,XX/47,XXX phenotype

Prenatal diagnosis, 1993-12, Vol.13 (12), p.1165-1166 [Peer Reviewed Journal]

Copyright © 1993 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970131219 ;PMID: 8177840

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19
Notes on African Euphorbiaceae XXX: Phyllanthus (V) &amp; c
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Notes on African Euphorbiaceae XXX: Phyllanthus (V) & c

Kew bulletin, 1996-01, Vol.51 (2), p.301-331 [Peer Reviewed Journal]

Copyright 1996 The Board of Trustees of The Royal Botanic Gardens, Kew ;ISSN: 0075-5974 ;EISSN: 1874-933X ;DOI: 10.2307/4119325

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20
Genetic counseling for sex chromosome abnormalities
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Genetic counseling for sex chromosome abnormalities

American journal of medical genetics, 2002-06, Vol.110 (1), p.3-10 [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.10391 ;PMID: 12116264 ;CODEN: AJMGDA

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