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European Journal of Human Genetics : EJHG
|
October 13, 2017
Responsible implementation of expanded carrier screening
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, et al.
European Journal of Human Genetics : EJHG
|
November 23, 2020
Opportunistic genomic screening. Recommendations of the European Society of Human Genetics
Guido de Wert, Wybo Dondorp, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
April 24, 2018
Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe
Fabio Sirchia, Daniele Carrieri, Sandi Dheensa, et al.
Journal of Medical Genetics
|
January 16, 2016
A specific mutation in TBL1XR1 causes Pierpont syndrome
Charlotte A Heinen, Aldo Jongejan, Peter J Watson, et al.
Human Mutation
|
April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and <i>SRRM2</i> Haploinsufficiency
Alistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.
European Journal of Human Genetics : EJHG
|
March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Wybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Wybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG
|
April 2, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations
Wybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG
|
October 13, 2018
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, et al.
International Journal of Molecular Sciences
|
February 3, 2021
Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS)
Valentina Guida, Luciano Calzari, Maria Teresa Fadda, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
October 13, 2017
Responsible implementation of expanded carrier screening
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, et al.
European Journal of Human Genetics : EJHG
|
November 23, 2020
Opportunistic genomic screening. Recommendations of the European Society of Human Genetics
Guido de Wert, Wybo Dondorp, Angus Clarke, et al.
European Journal of Human Genetics : EJHG
|
April 24, 2018
Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe
Fabio Sirchia, Daniele Carrieri, Sandi Dheensa, et al.
Journal of Medical Genetics
|
January 16, 2016
A specific mutation in TBL1XR1 causes Pierpont syndrome
Charlotte A Heinen, Aldo Jongejan, Peter J Watson, et al.
Human Mutation
|
April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and <i>SRRM2</i> Haploinsufficiency
Alistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.
European Journal of Human Genetics : EJHG
|
March 19, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Wybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Wybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG
|
April 2, 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations
Wybo Dondorp, Guido de Wert, Yvonne Bombard, et al.
European Journal of Human Genetics : EJHG
|
October 13, 2018
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, et al.
International Journal of Molecular Sciences
|
February 3, 2021
Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS)
Valentina Guida, Luciano Calzari, Maria Teresa Fadda, et al.
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of 8