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Lyn S Chitty

Showing results (121-130 of 225) with videos related to

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Prenatal Diagnosis|June 28, 2017
Promises, pitfalls and practicalities of prenatal whole exome sequencingSunayna Best, Karen Wou, Neeta Vora, et al.
Prenatal Diagnosis|March 3, 2026
Diagnostic Yield of Sequencing for Prenatal Diagnosis of Fetal Structural Anomalies: An Updated Systematic ReviewKaren Mei Xian Lim, Alexander Gibbs, Elizabeth Scotchman, et al.
Prenatal Diagnosis|August 16, 2015
Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalitiesSuzanne Drury, Hywel Williams, Natalie Trump, et al.
Prenatal Diagnosis|April 24, 2016
Non-invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathwaysTalitha I Verhoef, Melissa Hill, Suzanne Drury, et al.
Prenatal Diagnosis|July 29, 2006
Sonographic diagnosis of SEDC and double heterozygote of SEDC and achondroplasia--a report of six pregnanciesLyn S Chitty, Aileen W C Tan, Debbie L Nesbit, et al.
Clinical Genetics|July 20, 2019
Development of a measure of genome sequencing knowledge for young people: The kids-KOGSCeline Lewis, Bao S Loe, Chris Sidey-Gibbons, et al.
Prenatal Diagnosis|February 15, 2013
Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNALyn S Chitty, Asma Khalil, Angela N Barrett, et al.
Prenatal Diagnosis|August 29, 2013
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literatureJonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, et al.
Journal of Proteomics|May 1, 2012
The development of a peptide SRM-based tandem mass spectrometry assay for prenatal screening of Down syndromeWendy Heywood, Darrell Wang, Tracey E Madgett, et al.
FEBS Letters|May 6, 2006
Excess methionine suppresses the methylation cycle and inhibits neural tube closure in mouse embryosLouisa P E Dunlevy, Katie A Burren, Lyn S Chitty, et al.
Pageof 23

Showing results (121-130 of 225) with videos related to

Sort By:
Pageof 23
Prenatal Diagnosis|June 28, 2017
Promises, pitfalls and practicalities of prenatal whole exome sequencingSunayna Best, Karen Wou, Neeta Vora, et al.
Prenatal Diagnosis|March 3, 2026
Diagnostic Yield of Sequencing for Prenatal Diagnosis of Fetal Structural Anomalies: An Updated Systematic ReviewKaren Mei Xian Lim, Alexander Gibbs, Elizabeth Scotchman, et al.
Prenatal Diagnosis|August 16, 2015
Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalitiesSuzanne Drury, Hywel Williams, Natalie Trump, et al.
Prenatal Diagnosis|April 24, 2016
Non-invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathwaysTalitha I Verhoef, Melissa Hill, Suzanne Drury, et al.
Prenatal Diagnosis|July 29, 2006
Sonographic diagnosis of SEDC and double heterozygote of SEDC and achondroplasia--a report of six pregnanciesLyn S Chitty, Aileen W C Tan, Debbie L Nesbit, et al.
Clinical Genetics|July 20, 2019
Development of a measure of genome sequencing knowledge for young people: The kids-KOGSCeline Lewis, Bao S Loe, Chris Sidey-Gibbons, et al.
Prenatal Diagnosis|February 15, 2013
Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNALyn S Chitty, Asma Khalil, Angela N Barrett, et al.
Prenatal Diagnosis|August 29, 2013
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literatureJonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, et al.
Journal of Proteomics|May 1, 2012
The development of a peptide SRM-based tandem mass spectrometry assay for prenatal screening of Down syndromeWendy Heywood, Darrell Wang, Tracey E Madgett, et al.
FEBS Letters|May 6, 2006
Excess methionine suppresses the methylation cycle and inhibits neural tube closure in mouse embryosLouisa P E Dunlevy, Katie A Burren, Lyn S Chitty, et al.
Pageof 23