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1
10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France
10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France
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10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France

Orphanet journal of rare diseases, 2021-08, Vol.16 (1), p.1-345, Article 345 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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. ;Attribution ;The Author(s) 2021 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-021-01957-4 ;PMID: 34348744

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2
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
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118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

BMC medical genetics, 2009-06, Vol.10 (1), p.49-49, Article 49 [Peer Reviewed Journal]

COPYRIGHT 2009 BioMed Central Ltd. ;Copyright © 2009 Shaw et al; licensee BioMed Central Ltd. 2009 Shaw et al; licensee BioMed Central Ltd. ;ISSN: 1471-2350 ;EISSN: 1471-2350 ;DOI: 10.1186/1471-2350-10-49 ;PMID: 19493349

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3
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
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11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies

BMC medical genomics, 2021-04, Vol.14 (1), p.99-99, Article 99 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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) 2021 ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-021-00945-8 ;PMID: 33836758

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4
137Cs and 40K in gray seals Halichoerus grypus in the southern Baltic Sea
137Cs and 40K in gray seals Halichoerus grypus in the southern Baltic Sea
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137Cs and 40K in gray seals Halichoerus grypus in the southern Baltic Sea

Environmental science and pollution research international, 2019-06, Vol.26 (17), p.17418-17426 [Peer Reviewed Journal]

The Author(s) 2019 ;Environmental Science and Pollution Research is a copyright of Springer, (2019). All Rights Reserved. © 2019. 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: 0944-1344 ;EISSN: 1614-7499 ;DOI: 10.1007/s11356-019-05145-7 ;PMID: 31020531

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5
15d-prostaglandin J2 protects cortical neurons against oxygen-glucose deprivation/reoxygenation injury: involvement of inhibiting autophagy through upregulation of Bcl-2
15d-prostaglandin J2 protects cortical neurons against oxygen-glucose deprivation/reoxygenation injury: involvement of inhibiting autophagy through upregulation of Bcl-2
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15d-prostaglandin J2 protects cortical neurons against oxygen-glucose deprivation/reoxygenation injury: involvement of inhibiting autophagy through upregulation of Bcl-2

Cellular and molecular neurobiology, 2015-04, Vol.35 (3), p.303 [Peer Reviewed Journal]

EISSN: 1573-6830 ;DOI: 10.1007/s10571-014-0125-y ;PMID: 25349027

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6
16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up
16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up
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16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up

BMC pregnancy and childbirth, 2022-12, Vol.22 (1), p.913-913 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-022-05267-w ;PMID: 36476185

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7
17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype
17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype
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17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype

Orphanet journal of rare diseases, 2018-07, Vol.13 (1), p.106-106, Article 106 [Peer Reviewed Journal]

COPYRIGHT 2018 BioMed Central Ltd. ;COPYRIGHT 2018 BioMed Central Ltd. ;Copyright © 2018. 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). 2018 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-018-0838-y ;PMID: 29970136

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8
1945–1964 WHO’s Right to Health?
1945–1964 WHO’s Right to Health?
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1945–1964 WHO’s Right to Health?

Naturwissenschaften, Technik und Medizin, 2022-06, Vol.30 (2), p.137-165 [Peer Reviewed Journal]

The Author(s) 2022 ;2022. The Author(s). ;ISSN: 0036-6978 ;EISSN: 1420-9144 ;DOI: 10.1007/s00048-022-00333-y ;PMID: 35608615

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9
1H NMR-based metabolomics reveals the effect of maternal habitual dietary patterns on human amniotic fluid profile
1H NMR-based metabolomics reveals the effect of maternal habitual dietary patterns on human amniotic fluid profile
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1H NMR-based metabolomics reveals the effect of maternal habitual dietary patterns on human amniotic fluid profile

Scientific reports, 2018-03, Vol.8 (1), p.1-12, Article 4076 [Peer Reviewed Journal]

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. ;The Author(s) 2018 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-22230-y ;PMID: 29511239

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10
2019 Congress of the Italian Society of Neonatology
2019 Congress of the Italian Society of Neonatology
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2019 Congress of the Italian Society of Neonatology

Italian journal of pediatrics, 2019-12, Vol.45(Suppl 2) (S2), p.1-16 [Peer Reviewed Journal]

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. ;ISSN: 1720-8424 ;EISSN: 1824-7288 ;DOI: 10.1186/s13052-019-0729-4

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11
2021 recommendations of the Brazilian Society of Rheumatology for the gynecological and obstetric care of patients with Sjogren's syndrome
2021 recommendations of the Brazilian Society of Rheumatology for the gynecological and obstetric care of patients with Sjogren's syndrome
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2021 recommendations of the Brazilian Society of Rheumatology for the gynecological and obstetric care of patients with Sjogren's syndrome

Advances in rheumatology (London, England), 2021-09, Vol.61 (1), p.54-54, Article 54 [Peer Reviewed Journal]

2021. The Author(s). ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 2523-3106 ;EISSN: 2523-3106 ;DOI: 10.1186/s42358-021-00208-1 ;PMID: 34479630

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12
20α-Hydroxysteroid Dehydrogenase Expression in the Human Myometrium at Term and Preterm Birth: Relationships to Fetal Sex and Maternal Body Mass Index
20α-Hydroxysteroid Dehydrogenase Expression in the Human Myometrium at Term and Preterm Birth: Relationships to Fetal Sex and Maternal Body Mass Index
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20α-Hydroxysteroid Dehydrogenase Expression in the Human Myometrium at Term and Preterm Birth: Relationships to Fetal Sex and Maternal Body Mass Index

Reproductive sciences (Thousand Oaks, Calif.), 2023-08, Vol.30 (8), p.2512-2523 [Peer Reviewed Journal]

The Author(s) 2023 ;2023. The Author(s). ;ISSN: 1933-7191 ;EISSN: 1933-7205 ;DOI: 10.1007/s43032-023-01183-2 ;PMID: 36765000

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13
21st Annual Congress ESGE September 11-14, 2012, Paris
21st Annual Congress ESGE September 11-14, 2012, Paris
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21st Annual Congress ESGE September 11-14, 2012, Paris

Gynecological surgery, 2012-09, Vol.9 (Suppl 1), p.1-137 [Peer Reviewed Journal]

Springer-Verlag 2012 ;Springer-Verlag Berlin Heidelberg 2012 ;ISSN: 1613-2076 ;EISSN: 1613-2084 ;DOI: 10.1007/s10397-012-0767-z

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14
2D DIGE analysis of maternal plasma for potential biomarkers of Down Syndrome
2D DIGE analysis of maternal plasma for potential biomarkers of Down Syndrome
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2D DIGE analysis of maternal plasma for potential biomarkers of Down Syndrome

Proteome science, 2011-09, Vol.9 (1), p.56-56, Article 56 [Peer Reviewed Journal]

COPYRIGHT 2011 BioMed Central Ltd. ;2011 Heywood et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2011 Heywood et al; licensee BioMed Central Ltd. 2011 Heywood et al; licensee BioMed Central Ltd. ;ISSN: 1477-5956 ;EISSN: 1477-5956 ;DOI: 10.1186/1477-5956-9-56 ;PMID: 21929753

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15
2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study
2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study
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2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study

Journal of autism and developmental disorders, 2018-09, Vol.48 (9), p.3244-3252 [Peer Reviewed Journal]

The Author(s) 2018 ;COPYRIGHT 2018 Springer ;Journal of Autism and Developmental Disorders is a copyright of Springer, (2018). All Rights Reserved. © 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: 0162-3257 ;ISSN: 1573-3432 ;EISSN: 1573-3432 ;DOI: 10.1007/s10803-018-3588-8 ;PMID: 29704141

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16
2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria
2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria
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2D:4D Suggests a Role of Prenatal Testosterone in Gender Dysphoria

Archives of sexual behavior, 2020-02, Vol.49 (2), p.421-432 [Peer Reviewed Journal]

The Author(s) 2020 ;Archives of Sexual Behavior is a copyright of Springer, (2020). All Rights Reserved. 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: 0004-0002 ;EISSN: 1573-2800 ;DOI: 10.1007/s10508-020-01630-0 ;PMID: 31975034

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17
3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation
3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation
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3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation

Journal of cardiovascular magnetic resonance, 2022-12, Vol.24 (1), p.71-71 [Peer Reviewed Journal]

2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-022-00902-z ;PMID: 36517850

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18
3D brain Organoids derived from pluripotent stem cells: promising experimental models for brain development and neurodegenerative disorders
3D brain Organoids derived from pluripotent stem cells: promising experimental models for brain development and neurodegenerative disorders
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3D brain Organoids derived from pluripotent stem cells: promising experimental models for brain development and neurodegenerative disorders

Journal of biomedical science, 2017-08, Vol.24 (1), p.59-59, Article 59 [Peer Reviewed Journal]

COPYRIGHT 2017 BioMed Central Ltd. ;Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 1423-0127 ;ISSN: 1021-7770 ;EISSN: 1423-0127 ;DOI: 10.1186/s12929-017-0362-8 ;PMID: 28822354

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19
3D cephalometric analysis using Magnetic Resonance Imaging: validation of accuracy and reproducibility
3D cephalometric analysis using Magnetic Resonance Imaging: validation of accuracy and reproducibility
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3D cephalometric analysis using Magnetic Resonance Imaging: validation of accuracy and reproducibility

Scientific reports, 2018-08, Vol.8 (1), p.13029-11, Article 13029 [Peer Reviewed Journal]

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. ;The Author(s) 2018 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-018-31384-8 ;PMID: 30158656

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20
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome
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3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome

Molecular cytogenetics, 2014-09, Vol.7 (1), p.59-59, Article 59 [Peer Reviewed Journal]

COPYRIGHT 2014 BioMed Central Ltd. ;2014 Dupont et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. ;Dupont et al.; licensee BioMed Central Ltd. 2014 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-014-0059-6 ;PMID: 25320640

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