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1
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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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

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2
Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study
Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study
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Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study

Prenatal diagnosis, 2017-06, Vol.37 (6), p.583 [Peer Reviewed Journal]

2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5051 ;PMID: 28406537

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3
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses
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Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses

European journal of human genetics : EJHG, 2009-07, Vol.17 (7), p.897-903 [Peer Reviewed Journal]

2009 INIST-CNRS ;Copyright Nature Publishing Group Jul 2009 ;Copyright © 2009 Macmillan Publishers Limited 2009 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2008.265 ;PMID: 19156167

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4
Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies
Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies
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Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies

Genetics in medicine, 2019-11, Vol.21 (11), p.2462-2467 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0550-x ;PMID: 31123319

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5
Genetic syndromes associated with isolated fetal growth restriction
Genetic syndromes associated with isolated fetal growth restriction
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Genetic syndromes associated with isolated fetal growth restriction

Prenatal diagnosis, 2020-03, Vol.40 (4), p.432 [Peer Reviewed Journal]

2019 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5635 ;PMID: 31891188

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6
Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases
Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases
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Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases

Journal of assisted reproduction and genetics, 2018-02, Vol.35 (2), p.265-271 [Peer Reviewed Journal]

Springer Science+Business Media, LLC 2017 ;Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2017). All Rights Reserved. ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-017-1069-1 ;PMID: 29086320

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7
Gene-environment interactions and their impact on human health
Gene-environment interactions and their impact on human health
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Gene-environment interactions and their impact on human health

Genes and immunity, 2023-02, Vol.24 (1), p.1-11 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. 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: 1476-5470 ;ISSN: 1466-4879 ;EISSN: 1476-5470 ;DOI: 10.1038/s41435-022-00192-6 ;PMID: 36585519

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8
Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review
Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review
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Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review

Prenatal diagnosis, 2017-11, Vol.37 (11), p.1061 [Peer Reviewed Journal]

2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5160 ;PMID: 28944967

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9
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
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Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.521-526 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group May 2012 ;Copyright © 2012 Macmillan Publishers Limited 2012 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2011.246 ;PMID: 22234154

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10
Differential Gene Expression in Articular Cartilage and Subchondral Bone of Neonatal and Adult Horses
Differential Gene Expression in Articular Cartilage and Subchondral Bone of Neonatal and Adult Horses
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Differential Gene Expression in Articular Cartilage and Subchondral Bone of Neonatal and Adult Horses

Genes, 2019-09, Vol.10 (10), p.745 [Peer Reviewed Journal]

2019 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 (http://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. ;2019 by the authors. 2019 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes10100745 ;PMID: 31557843

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11
Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients
Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients
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Long-term follow-up in primary Sjögren's syndrome reveals differences in clinical presentation between female and male patients

Biology of sex differences, 2017-08, Vol.8 (1), p.25-25, Article 25 [Peer Reviewed Journal]

Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 2042-6410 ;EISSN: 2042-6410 ;DOI: 10.1186/s13293-017-0146-6 ;PMID: 28789696

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12
Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations
Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations
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Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations

Journal of human genetics, 2015-03, Vol.60 (3), p.133-137 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2015 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2014.116 ;PMID: 25566756

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13
Genetic analysis of products of conception using a HLPA/SNP-array strategy
Genetic analysis of products of conception using a HLPA/SNP-array strategy
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Genetic analysis of products of conception using a HLPA/SNP-array strategy

Molecular cytogenetics, 2019-09, Vol.12 (1), p.40-40, Article 40 [Peer Reviewed Journal]

The Author(s). 2019. ;COPYRIGHT 2019 BioMed Central Ltd. ;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: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-019-0452-2 ;PMID: 31687045

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14
Brief co-incubation of gametes benefits the outcomes of newborns
Brief co-incubation of gametes benefits the outcomes of newborns
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Brief co-incubation of gametes benefits the outcomes of newborns

Journal of assisted reproduction and genetics, 2018-08, Vol.35 (8), p.1537-1542 [Peer Reviewed Journal]

Springer Science+Business Media, LLC, part of Springer Nature 2018 ;Journal of Assisted Reproduction and Genetics is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 1058-0468 ;EISSN: 1573-7330 ;DOI: 10.1007/s10815-018-1229-y ;PMID: 29926375

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15
X chromosome abnormal inactivation: a unique factor for women's diseases?
X chromosome abnormal inactivation: a unique factor for women's diseases?
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X chromosome abnormal inactivation: a unique factor for women's diseases?

Epigenomics, 2016-04, Vol.8 (4), p.447-450 [Peer Reviewed Journal]

Future Medicine Ltd ;Copyright Future Medicine Ltd Apr 2016 ;ISSN: 1750-1911 ;EISSN: 1750-192X ;DOI: 10.2217/epi.16.2 ;PMID: 27032507

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16
Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China
Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China
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Presence of chromosomal abnormalities in fetuses with isolated ventriculomegaly on prenatal ultrasound in China

Molecular genetics & genomic medicine, 2018-11, Vol.6 (6), p.1015-1020 [Peer Reviewed Journal]

2018 The Authors. published by Wiley Periodicals, Inc. ;2018 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;2018. 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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.477 ;PMID: 30230267

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17
Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis
Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis
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Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis

European journal of human genetics : EJHG, 2004-07, Vol.12 (7), p.513-520 [Peer Reviewed Journal]

2004 INIST-CNRS ;Copyright Nature Publishing Group Jul 2004 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201178 ;PMID: 15054396

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