Results 1 - 20 of 956 for All Library Resources
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Material Type: Article
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Aging and aneuploidy: evidence for the preferential involvement of the inactive X chromosomeCytogenetic and genome research, 1985, Vol.39 (4), p.275-278 [Peer Reviewed Journal]1985 S. Karger AG, Basel ;1986 INIST-CNRS ;ISSN: 1424-8581 ;ISSN: 0301-0171 ;EISSN: 1424-859X ;DOI: 10.1159/000132157 ;PMID: 4053692 ;CODEN: CGCGBRDigital Resources/Online E-Resources |
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Etiology of nondisjunction in humansEnvironmental and molecular mutagenesis, 1995, Vol.25 (S2), p.38-47 [Peer Reviewed Journal]Copyright © 1995 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0893-6692 ;EISSN: 1098-2280 ;DOI: 10.1002/em.2850250608 ;PMID: 7789361Full text available |
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Mosaic Turner syndrome: cytogenetics versus FISHAnnals of human genetics, 1999-05, Vol.63 (3), p.199-206 [Peer Reviewed Journal]University College London 1999 ;1999 University College London ;1999 INIST-CNRS ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1046/j.1469-1809.1999.6330199.x ;PMID: 10738532 ;CODEN: ANHGAAFull text available |
| 4 |
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Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for fragile X syndromeGenetic testing, 2003-12, Vol.7 (4), p.345ISSN: 1090-6576 ;EISSN: 1557-7473 ;DOI: 10.1089/109065703322783734 ;PMID: 15000814Digital Resources/Online E-Resources |
| 5 |
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Turner syndrome and 45,X/47,XXX mosaicismGenetic counseling, 2009-01, Vol.20 (2), p.141-146 [Peer Reviewed Journal]Copyright Éditions Médecine et Hygiène 2009 ;ISSN: 1015-8146 ;PMID: 19650411Full text available |
| 6 |
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Silencing XIST on the future active X: Searching human and bovine preimplantation embryos for the repressorEuropean journal of human genetics : EJHG, 2024-04, Vol.32 (4), p.399-406 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to European Society of Human Genetics. ;The Author(s), under exclusive licence to European Society of Human Genetics 2022. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-022-01115-9 ;PMID: 35585273Full text available |
| 7 |
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Ullrich-turner syndrome in monozygotic twinsAmerican journal of medical genetics, 1983-08, Vol.15 (4), p.537-542 [Peer Reviewed Journal]Copyright © 1983 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320150403 ;PMID: 6684396Full text available |
| 8 |
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Nearly a third of abnormalities found after first-trimester screening are different than expected:10-year experience from a single centerPrenatal diagnosis, 2013-03, Vol.33 (3), p.251-256 [Peer Reviewed Journal]2013 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4054 ;PMID: 23354915Full text available |
| 9 |
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Cytological and epidemiological findings in trisomies 13, 18, and 21: England and Wales 2004-2009American journal of medical genetics. Part A, 2012-05, Vol.158A (5), p.1145-1150 [Peer Reviewed Journal]Copyright © 2012 Wiley Periodicals, Inc. ;2015 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.35337 ;PMID: 22495937Full text available |
| 10 |
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Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidiesGenetics in medicine, 2011-02, Vol.13 (2), p.140-147 [Peer Reviewed Journal]2011 The Author(s) ;The American College of Medical Genetics 2011. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1097/GIM.0b013e3182036763 ;PMID: 21233717Full text available |
| 11 |
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Constitutional Trisomy 8 Mosaicism with Persistent MacrocytosisCytogenetic and genome research, 2016-01, Vol.150 (1), p.35-39 [Peer Reviewed Journal]2016 S. Karger AG, Basel ;2016 S. Karger AG, Basel. ;ISSN: 1424-8581 ;EISSN: 1424-859X ;DOI: 10.1159/000452358 ;PMID: 27838684Digital Resources/Online E-Resources |
| 12 |
Material Type: Article
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Epigenetics in Turner syndromeClinical epigenetics, 2018-04, Vol.10 (1), p.45-45, Article 45 [Peer Reviewed Journal]COPYRIGHT 2018 BioMed Central Ltd. ;The Author(s). 2018 ;ISSN: 1868-7075 ;EISSN: 1868-7083 ;DOI: 10.1186/s13148-018-0477-0 ;PMID: 29636833Full text available |
| 13 |
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Frequent gain of chromosome 19 in megakaryoblastic leukemias detected by comparative genomic hybridizationGenes chromosomes & cancer, 2001-11, Vol.32 (3), p.285-293 [Peer Reviewed Journal]Copyright © 2001 Wiley‐Liss, Inc. ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 1045-2257 ;EISSN: 1098-2264 ;DOI: 10.1002/gcc.1192 ;PMID: 11579469Full text available |
| 14 |
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47,XXX females, sex chromosomes, and tooth crown structureHuman genetics, 1987-12, Vol.77 (4), p.345-348 [Peer Reviewed Journal]ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00291424 ;PMID: 3692479Full text available |
| 15 |
Material Type: Article
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Taurodontism and the Presence of an Extra Y Chromosome: Study of 47,XYY Males and Analytical ReviewHuman biology, 1991-02, Vol.63 (1), p.31-38 [Peer Reviewed Journal]Copyright © 1991 Wayne State University Press ;1992 INIST-CNRS ;Copyright Wayne State University Press Feb 1991 ;ISSN: 0018-7143 ;EISSN: 1534-6617 ;PMID: 2004742 ;CODEN: HUBIAADigital Resources/Online E-Resources |
| 16 |
Material Type: Article
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THE AGE OF MENOPAUSE IN CLASSICAL GREECE AND ROMEHuman biology, 1970-02, Vol.42 (1), p.79-86 [Peer Reviewed Journal]Copyright 1970 Wayne State University Press ;ISSN: 0018-7143 ;EISSN: 1534-6617 ;PMID: 4910710Digital Resources/Online E-Resources |
| 17 |
Material Type: Article
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THE AGE OF MENARCHE IN CLASSICAL GREECE AND ROMEHuman biology, 1969-02, Vol.41 (1), p.125-132 [Peer Reviewed Journal]Copyright 1969 Wayne State University Press ;ISSN: 0018-7143 ;EISSN: 1534-6617 ;PMID: 4891546 ;CODEN: HUBIAADigital Resources/Online E-Resources |
| 18 |
Material Type: Article
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Cytogenetic Investigation of Infertile Patients in Hungary: A 10-Year Retrospective StudyGenes, 2022-11, Vol.13 (11), p.2086 [Peer Reviewed Journal]COPYRIGHT 2022 MDPI AG ;2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes13112086 ;PMID: 36360324Full text available |
| 19 |
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A boy with true hermaphroditism and sex chromosome mosaicism and a fertile woman with Turner mosaicism in a family with a translocation 8p:19pClinical genetics, 1981-10, Vol.20 (4), p.289-295 [Peer Reviewed Journal]ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1981.tb01035.x ;PMID: 7333022Full text available |
| 20 |
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Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsGenetics in medicine, 2018-05, Vol.20 (5), p.513-523 [Peer Reviewed Journal]Copyright Nature Publishing Group May 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.134 ;PMID: 29261177Full text available |
Results 1 - 20 of 956 for All Library Resources
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