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European Journal of Medical Genetics
|
May 16, 2019
Update on the use of exome sequencing in the diagnosis of fetal abnormalities
Lauren Ferretti, Rhiannon Mellis, Lyn S Chitty
Prenatal Diagnosis
|
September 20, 2014
'Hope for safe prenatal gene tests'. A content analysis of how the UK press media are reporting advances in non-invasive prenatal testing
Celine Lewis, Mahrufa Choudhury, Lyn S Chitty
Current Opinion in Obstetrics & Gynecology
|
February 12, 2016
Stakeholder attitudes and needs regarding cell-free fetal DNA testing
Melissa Hill, Celine Lewis, Lyn S Chitty
Prenatal Diagnosis
|
September 12, 2017
Offering non-invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
Celine Lewis, Melissa Hill, Lyn S Chitty
Cold Spring Harbor Perspectives in Medicine
|
July 19, 2015
Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNA
Lyn S Chitty, Y M Dennis Lo
Expert Review of Molecular Diagnostics
|
July 3, 2018
Next-generation sequencing and the impact on prenatal diagnosis
Rhiannon Mellis, Natalie Chandler, Lyn S Chitty
Prenatal Diagnosis
|
September 14, 2024
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use"
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Prenatal Diagnosis
|
November 22, 2023
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Prenatal Diagnosis
|
November 4, 2015
Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus?
Lyn S Chitty, Jan M Friedman, Sylvie Langlois
Prenatal Diagnosis
|
February 9, 2018
Current controversies in prenatal diagnosis 2: Cell-free DNA prenatal screening should be used to identify all chromosome abnormalities
Lyn S Chitty, Louanne Hudgins, Mary E Norton
Page
of 23
Search research articles
Search
Showing results (41-50 of 225) with videos related to
Sort By:
Page
of 23
European Journal of Medical Genetics
|
May 16, 2019
Update on the use of exome sequencing in the diagnosis of fetal abnormalities
Lauren Ferretti, Rhiannon Mellis, Lyn S Chitty
Prenatal Diagnosis
|
September 20, 2014
'Hope for safe prenatal gene tests'. A content analysis of how the UK press media are reporting advances in non-invasive prenatal testing
Celine Lewis, Mahrufa Choudhury, Lyn S Chitty
Current Opinion in Obstetrics & Gynecology
|
February 12, 2016
Stakeholder attitudes and needs regarding cell-free fetal DNA testing
Melissa Hill, Celine Lewis, Lyn S Chitty
Prenatal Diagnosis
|
September 12, 2017
Offering non-invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
Celine Lewis, Melissa Hill, Lyn S Chitty
Cold Spring Harbor Perspectives in Medicine
|
July 19, 2015
Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNA
Lyn S Chitty, Y M Dennis Lo
Expert Review of Molecular Diagnostics
|
July 3, 2018
Next-generation sequencing and the impact on prenatal diagnosis
Rhiannon Mellis, Natalie Chandler, Lyn S Chitty
Prenatal Diagnosis
|
September 14, 2024
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use"
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Prenatal Diagnosis
|
November 22, 2023
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Prenatal Diagnosis
|
November 4, 2015
Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus?
Lyn S Chitty, Jan M Friedman, Sylvie Langlois
Prenatal Diagnosis
|
February 9, 2018
Current controversies in prenatal diagnosis 2: Cell-free DNA prenatal screening should be used to identify all chromosome abnormalities
Lyn S Chitty, Louanne Hudgins, Mary E Norton
Page
of 23